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nsv5467984

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,843

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 175 SVs from 54 studies. See in: genome view    
Submitted genomic12,237,692-12,244,534Question Mark
Overlapping variant regions from other studies: 175 SVs from 54 studies. See in: genome view    
Remapped(Score: Perfect):12,277,318-12,284,160Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5467984Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr712,237,69212,244,534
nsv5467984RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr712,277,31812,284,160

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16993035deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16993035Submitted genomicNC_000007.14:g.122
37692_12244534del
GRCh38 (hg38)NC_000007.14Chr712,237,69212,244,534
nssv16993035RemappedPerfectNC_000007.13:g.122
77318_12284160del
GRCh37.p13First PassNC_000007.13Chr712,277,31812,284,160

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)
nssv16993035<0.00126402
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