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nsv5534000

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 23 studies. See in: genome view    
Submitted genomic141,570,235-141,570,273Question Mark
Overlapping variant regions from other studies: 124 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):141,270,035-141,270,073Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5534000Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7141,570,235141,570,273
nsv5534000RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7141,270,035141,270,073

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004440insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004440Submitted genomicNC_000007.14:g.141
570235_141570273in
s319
GRCh38 (hg38)NC_000007.14Chr7141,570,235141,570,273
nssv17004440RemappedPerfectNC_000007.13:g.141
270035_141270073in
s319
GRCh37.p13First PassNC_000007.13Chr7141,270,035141,270,073

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)
nssv17004440<0.00116404
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