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nsv3167821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74,156

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 324 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):135,728,747-135,802,916Question Mark
Overlapping variant regions from other studies: 324 SVs from 35 studies. See in: genome view    
Submitted genomic136,740,990-136,815,159Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3167821RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8135,728,754 (-7, +7)135,802,909 (-7, +7)
nsv3167821Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8136,740,997 (-7, +7)136,815,152 (-7, +7)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14239289deletionDB110SequencingPaired-end mapping35

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14239289RemappedPerfectNC_000008.11:g.(13
5728747_135728761)
_(135802902_135802
916)del
GRCh38.p12First PassNC_000008.11Chr8135,728,754 (-7, +7)135,802,909 (-7, +7)
nssv14239289Submitted genomicNC_000008.10:g.(13
6740990_136741004)
_(136815145_136815
159)del
GRCh37 (hg19)NC_000008.10Chr8136,740,997 (-7, +7)136,815,152 (-7, +7)

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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