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nsv6138552

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 240 SVs from 50 studies. See in: genome view    
Submitted genomic13,276,384-13,282,384Question Mark
Overlapping variant regions from other studies: 567 SVs from 64 studies. See in: genome view    
Remapped(Score: Good):12,979,220-12,985,221Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6138552Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr113,276,38413,282,384
nsv6138552RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr112,979,22012,985,221

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894613duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894613Submitted genomicNC_000001.11:g.132
76384_13282384dup
GRCh38 (hg38)NC_000001.11Chr113,276,38413,282,384
nssv16894613RemappedGoodNC_000001.10:g.129
79220_12985221dup
GRCh37.p13First PassNC_000001.10Chr112,979,22012,985,221

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)
nssv168946130.0631512412
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