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nsv396554

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,647

Genome View

Select assembly:
Overlapping variant regions from other studies: 218 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):137,874,552-137,884,198Question Mark
Overlapping variant regions from other studies: 218 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):138,886,795-138,896,441Question Mark
Overlapping variant regions from other studies: 7 SVs from 2 studies. See in: genome view    
Submitted genomic138,955,977-138,965,623Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv396554RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8137,874,552137,884,198
nsv396554RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8138,886,795138,896,441
nsv396554Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000008.9Chr8138,955,977138,965,623

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv415132deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv415132RemappedPerfectNC_000008.11:g.137
874552_137884198de
l9647
GRCh38.p12First PassNC_000008.11Chr8137,874,552137,884,198
nssv415132RemappedPerfectNC_000008.10:g.138
886795_138896441de
l9647
GRCh37.p13First PassNC_000008.10Chr8138,886,795138,896,441
nssv415132Submitted genomicNC_000008.9:g.1389
55977_138965623del
9647
NCBI35 (hg17)NC_000008.9Chr8138,955,977138,965,623

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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