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nsv5487127

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,151

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 35 studies. See in: genome view    
Submitted genomic116,953,912-116,958,062Question Mark
Overlapping variant regions from other studies: 148 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):116,593,966-116,598,116Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487127Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7116,953,912116,958,062
nsv5487127RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7116,593,966116,598,116

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001428deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001428Submitted genomicNC_000007.14:g.116
953912_116958062de
l
GRCh38 (hg38)NC_000007.14Chr7116,953,912116,958,062
nssv17001428RemappedPerfectNC_000007.13:g.116
593966_116598116de
l
GRCh37.p13First PassNC_000007.13Chr7116,593,966116,598,116

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17001428<0.00116404
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