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nsv6246205

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
Submitted genomic79,852,656-79,852,656Question Mark
Overlapping variant regions from other studies: 145 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):80,764,891-80,764,891Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6246205Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr879,852,65679,852,656
nsv6246205RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr880,764,89180,764,891

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17839929alu insertionSequencingSplit read mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17839929Submitted genomicNC_000008.11:g.798
52656_79852657ins2
81
GRCh38 (hg38)NC_000008.11Chr879,852,65679,852,656
nssv17839929RemappedPerfectNC_000008.10:g.807
64891_80764892ins2
81
GRCh37.p13First PassNC_000008.10Chr880,764,89180,764,891

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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