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nsv5532815

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88,841

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 309 SVs from 36 studies. See in: genome view    
Submitted genomic66,940,488-67,029,328Question Mark
Overlapping variant regions from other studies: 309 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):66,974,391-67,063,231Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5532815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1666,940,48867,029,328
nsv5532815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1666,974,39167,063,231

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17709119duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17709119Submitted genomicNC_000016.10:g.669
40488_67029328dup
GRCh38 (hg38)NC_000016.10Chr1666,940,48867,029,328
nssv17709119RemappedPerfectNC_000016.9:g.6697
4391_67063231dup
GRCh37.p13First PassNC_000016.9Chr1666,974,39167,063,231

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)
nssv17709119<0.00136404
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