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nsv6141232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:353,106

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 968 SVs from 77 studies. See in: genome view    
Submitted genomic103,513,790-103,866,895Question Mark
Overlapping variant regions from other studies: 968 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):103,961,665-104,314,770Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6141232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6103,513,790103,866,895
nsv6141232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6103,961,665104,314,770

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16986219duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16986219Submitted genomicNC_000006.12:g.103
513790_103866895du
p
GRCh38 (hg38)NC_000006.12Chr6103,513,790103,866,895
nssv16986219RemappedPerfectNC_000006.11:g.103
961665_104314770du
p
GRCh37.p13First PassNC_000006.11Chr6103,961,665104,314,770

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)
nssv16986219<0.00116402
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