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nsv6280884

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
Submitted genomic105,561,504-105,561,504Question Mark
Overlapping variant regions from other studies: 136 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):106,482,661-106,482,661Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6280884Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4105,561,504105,561,504
nsv6280884RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4106,482,661106,482,661

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17882653insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17882653Submitted genomicNC_000004.12:g.105
561504_105561505in
s55
GRCh38 (hg38)NC_000004.12Chr4105,561,504105,561,504
nssv17882653RemappedPerfectNC_000004.11:g.106
482661_106482662in
s55
GRCh37.p13First PassNC_000004.11Chr4106,482,661106,482,661

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)
nssv17882653<0.00112322
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