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nsv482521

  • Variant Calls:16
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:177,904

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 694 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):101,960,722-102,138,625Question Mark
Overlapping variant regions from other studies: 434 SVs from 57 studies. See in: genome view    
Remapped(Score: Pass):101,604,002-101,718,950Question Mark
Submitted genomic101,164,183-101,342,086Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv482521RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7101,960,722102,138,625
nsv482521RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7101,604,002101,718,950
nsv482521Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000007.10Chr7101,164,183101,342,086

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3005923copy number lossBAC aCGHProbe signal intensity
nssv3006413copy number lossBAC aCGHProbe signal intensity
nssv3006669copy number lossBAC aCGHProbe signal intensity
nssv3006755copy number lossBAC aCGHProbe signal intensity
nssv3007283copy number lossBAC aCGHProbe signal intensity
nssv3007593copy number lossBAC aCGHProbe signal intensity
nssv3007961copy number lossBAC aCGHProbe signal intensity
nssv3008158copy number lossBAC aCGHProbe signal intensity
nssv3008309copy number lossBAC aCGHProbe signal intensity
nssv3008637copy number lossBAC aCGHProbe signal intensity
nssv3008748copy number lossBAC aCGHProbe signal intensity
nssv3009271copy number lossBAC aCGHProbe signal intensity
nssv3009444copy number lossBAC aCGHProbe signal intensity
nssv3010204copy number lossBAC aCGHProbe signal intensity
nssv3010210copy number lossBAC aCGHProbe signal intensity
nssv3010556copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3005923RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3006413RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3006669RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3006755RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3007283RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3007593RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3007961RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3008158RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3008309RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3008637RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3008748RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3009271RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3009444RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3010204RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3010210RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3010556RemappedPerfectNC_000007.14:g.(?_
101960722)_(102138
625_?)del
GRCh38.p12First PassNC_000007.14Chr7101,960,722102,138,625
nssv3005923RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3006413RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3006669RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3006755RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3007283RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3007593RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3007961RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3008158RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3008309RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3008637RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3008748RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3009271RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3009444RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3010204RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3010210RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3010556RemappedPassNC_000007.13:g.(?_
101604002)_(101718
950_?)del
GRCh37.p13First PassNC_000007.13Chr7101,604,002101,718,950
nssv3005923Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3006413Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3006669Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3006755Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3007283Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3007593Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3007961Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3008158Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3008309Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3008637Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3008748Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3009271Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3009444Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3010204Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3010210Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086
nssv3010556Submitted genomicNC_000007.10:g.(?_
101164183)_(101342
086_?)del
NCBI34 (hg16)NC_000007.10Chr7101,164,183101,342,086

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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