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nsv5895099

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:721

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
Submitted genomic118,243,072-118,243,792Question Mark
Overlapping variant regions from other studies: 154 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):118,564,235-118,564,955Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5895099Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6118,243,072118,243,792
nsv5895099RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6118,564,235118,564,955

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17425107deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17425107Submitted genomicNC_000006.12:g.118
243072_118243792de
l
GRCh38 (hg38)NC_000006.12Chr6118,243,072118,243,792
nssv17425107RemappedPerfectNC_000006.11:g.118
564235_118564955de
l
GRCh37.p13First PassNC_000006.11Chr6118,564,235118,564,955

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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