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nsv834023

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:219,914

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 990 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):60,942,891-61,162,804Question Mark
Overlapping variant regions from other studies: 990 SVs from 90 studies. See in: genome view    
Remapped(Score: Perfect):59,517,947-59,737,860Question Mark
Overlapping variant regions from other studies: 101 SVs from 11 studies. See in: genome view    
Submitted genomic58,951,342-59,171,255Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv834023RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2060,942,89161,162,804
nsv834023RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2059,517,94759,737,860
nsv834023Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000020.9Chr2058,951,34259,171,255

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1455156copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1455156RemappedPerfectNC_000020.11:g.(60
942891_?)_(?_61162
804)del
GRCh38.p12First PassNC_000020.11Chr2060,942,89161,162,804
nssv1455156RemappedPerfectNC_000020.10:g.(59
517947_?)_(?_59737
860)del
GRCh37.p13First PassNC_000020.10Chr2059,517,94759,737,860
nssv1455156Submitted genomicNC_000020.9:g.(589
51342_?)_(?_591712
55)del
NCBI35 (hg17)NC_000020.9Chr2058,951,34259,171,255

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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