nsv6142995

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,501

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 39 studies. See in: genome view    
Submitted genomic9,654,000-9,659,500Question Mark
Overlapping variant regions from other studies: 97 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):9,675,547-9,681,047Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6142995Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr119,654,0009,659,500
nsv6142995RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr119,675,5479,681,047

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041275deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041275Submitted genomicNC_000011.10:g.965
4000_9659500del
GRCh38 (hg38)NC_000011.10Chr119,654,0009,659,500
nssv17041275RemappedPerfectNC_000011.9:g.9675
547_9681047del
GRCh37.p13First PassNC_000011.9Chr119,675,5479,681,047

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)
nssv17041275<0.00136384
Support Center