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nsv174

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,697

Genome View

Select assembly:
Overlapping variant regions from other studies: 470 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):36,340,817-36,374,513Question Mark
Overlapping variant regions from other studies: 470 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):36,831,719-36,865,415Question Mark
Overlapping variant regions from other studies: 5 SVs from 3 studies. See in: genome view    
Submitted genomic41,523,559-41,557,255Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv174RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1936,340,81736,374,513
nsv174RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,831,71936,865,415
nsv174Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000019.8Chr1941,523,55941,557,255

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv174deletionSAMN00000376SequencingPaired-end mapping297

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv174RemappedPerfectNC_000019.10:g.(36
340817_?)_(?_36374
513)del
GRCh38.p12First PassNC_000019.10Chr1936,340,81736,374,513
nssv174RemappedPerfectNC_000019.9:g.(368
31719_?)_(?_368654
15)del
GRCh37.p13First PassNC_000019.9Chr1936,831,71936,865,415
nssv174Submitted genomicNC_000019.8:g.(415
23559_?)_(?_415572
55)del10296
NCBI35 (hg17)NC_000019.8Chr1941,523,55941,557,255

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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