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nsv6268238

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:287

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 210 SVs from 34 studies. See in: genome view    
Submitted genomic155,335,437-155,335,723Question Mark
Overlapping variant regions from other studies: 210 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):155,127,659-155,127,945Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6268238Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7155,335,437155,335,723
nsv6268238RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7155,127,659155,127,945

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17884918deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17884918Submitted genomicNC_000007.14:g.155
335437_155335723de
l
GRCh38 (hg38)NC_000007.14Chr7155,335,437155,335,723
nssv17884918RemappedPerfectNC_000007.13:g.155
127659_155127945de
l
GRCh37.p13First PassNC_000007.13Chr7155,127,659155,127,945

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)
nssv17884918<0.00112340
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