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nsv5599684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,492

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 425 SVs from 53 studies. See in: genome view    
Submitted genomic43,739,501-43,740,992Question Mark
Overlapping variant regions from other studies: 425 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):45,159,382-45,160,873Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5599684Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2143,739,50143,740,992
nsv5599684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2145,159,38245,160,873

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17118683deletionHG01114SequencingSequence alignment977

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17118683Submitted genomicNC_000021.9:g.4373
9501_43740992delT
GRCh38 (hg38)NC_000021.9Chr2143,739,50143,740,992
nssv17118683RemappedPerfectNC_000021.8:g.4515
9382_45160873delT
GRCh37.p13First PassNC_000021.8Chr2145,159,38245,160,873

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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