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nsv5913497

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,849,877

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1997 SVs from 89 studies. See in: genome view    
Submitted genomic60,121,658-61,971,534Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeAssemblyAssembly UnitSequence IDChrStartStop
nsv5913497Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr760,121,65861,971,534

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17431609deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeHGVSAssemblySequence IDChrStartStop
nssv17431609Submitted genomicNC_000007.14:g.601
21658_61971534del
GRCh38 (hg38)NC_000007.14Chr760,121,65861,971,534

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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