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nsv6142967

  • 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: 76 SVs from 23 studies. See in: genome view    
Submitted genomic22,949,713-22,955,713Question Mark
Overlapping variant regions from other studies: 76 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):23,418,922-23,424,922Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6142967Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1422,949,71322,955,713
nsv6142967RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1423,418,92223,424,922

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17693942duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17693942Submitted genomicNC_000014.9:g.2294
9713_22955713dup
GRCh38 (hg38)NC_000014.9Chr1422,949,71322,955,713
nssv17693942RemappedPerfectNC_000014.8:g.2341
8922_23424922dup
GRCh37.p13First PassNC_000014.8Chr1423,418,92223,424,922

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)
nssv17693942<0.00126350
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