nsv5436982

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,602,627

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 11262 SVs from 122 studies. See in: genome view    
Submitted genomic85,539,948-89,142,574Question Mark
Overlapping variant regions from other studies: 11272 SVs from 122 studies. See in: genome view    
Remapped(Score: Good):85,767,071-89,442,057Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436982Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr285,539,94889,142,574
nsv5436982RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr285,767,07189,442,057

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917355deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917355Submitted genomicNC_000002.12:g.855
39948_89142574del
GRCh38 (hg38)NC_000002.12Chr285,539,94889,142,574
nssv16917355RemappedGoodNC_000002.11:g.857
67071_89442057del
GRCh37.p13First PassNC_000002.11Chr285,767,07189,442,057

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)
nssv16917355<0.00116404
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