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nsv5527780

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,480

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 188 SVs from 35 studies. See in: genome view    
Submitted genomic41,033,482-41,038,961Question Mark
Overlapping variant regions from other studies: 186 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):39,189,734-39,195,213Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5527780Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,033,48241,038,961
nsv5527780RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,189,73439,195,213

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713141deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713141Submitted genomicNC_000017.11:g.410
33482_41038961del
GRCh38 (hg38)NC_000017.11Chr1741,033,48241,038,961
nssv17713141RemappedPerfectNC_000017.10:g.391
89734_39195213del
GRCh37.p13First PassNC_000017.10Chr1739,189,73439,195,213

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)
nssv17713141<0.00146404
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