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nsv5651813

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 39 studies. See in: genome view    
Submitted genomic88,127,094-88,127,094Question Mark
Overlapping variant regions from other studies: 151 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):88,520,871-88,520,871Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5651813Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1288,127,09488,127,094
nsv5651813RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1288,520,87188,520,871

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17084162insertionSAMN00006579SequencingSequence alignment23,265

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17084162Submitted genomicNC_000012.12:g.881
27094_88127095ins7
0
GRCh38 (hg38)NC_000012.12Chr1288,127,09488,127,094
nssv17084162RemappedPerfectNC_000012.11:g.885
20871_88520872ins7
0
GRCh37.p13First PassNC_000012.11Chr1288,520,87188,520,871

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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