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nsv5511927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,806

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 418 SVs from 62 studies. See in: genome view    
Submitted genomic43,024,528-43,034,333Question Mark
Overlapping variant regions from other studies: 418 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):43,598,664-43,608,469Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5511927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1343,024,52843,034,333
nsv5511927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1343,598,66443,608,469

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17687265duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17687265Submitted genomicNC_000013.11:g.430
24528_43034333dup
GRCh38 (hg38)NC_000013.11Chr1343,024,52843,034,333
nssv17687265RemappedPerfectNC_000013.10:g.435
98664_43608469dup
GRCh37.p13First PassNC_000013.10Chr1343,598,66443,608,469

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)
nssv176872650.0452866404
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