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nsv5538615

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 192 SVs from 31 studies. See in: genome view    
Submitted genomic167,131,012-167,131,023Question Mark
Overlapping variant regions from other studies: 192 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):167,544,500-167,544,511Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5538615Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6167,131,012167,131,023
nsv5538615RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6167,544,500167,544,511

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16991256insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16991256Submitted genomicNC_000006.12:g.167
131012_167131023in
s86
GRCh38 (hg38)NC_000006.12Chr6167,131,012167,131,023
nssv16991256RemappedPerfectNC_000006.11:g.167
544500_167544511in
s86
GRCh37.p13First PassNC_000006.11Chr6167,544,500167,544,511

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)
nssv169912560.008526338
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