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nsv5461151

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:727,491

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2057 SVs from 103 studies. See in: genome view    
Submitted genomic159,927,300-160,654,790Question Mark
Overlapping variant regions from other studies: 2057 SVs from 103 studies. See in: genome view    
Remapped(Score: Perfect):160,348,332-161,075,822Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5461151Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6159,927,300160,654,790
nsv5461151RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6160,348,332161,075,822

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16989224duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16989224Submitted genomicNC_000006.12:g.159
927300_160654790du
p
GRCh38 (hg38)NC_000006.12Chr6159,927,300160,654,790
nssv16989224RemappedPerfectNC_000006.11:g.160
348332_161075822du
p
GRCh37.p13First PassNC_000006.11Chr6160,348,332161,075,822

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)
nssv16989224<0.00116404
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