nsv471332

  • Variant Calls:3
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:127,717

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1760 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):687,886-815,602Question Mark
Overlapping variant regions from other studies: 1760 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):688,001-815,717Question Mark
Overlapping variant regions from other studies: 191 SVs from 12 studies. See in: genome view    
Submitted genomic741,001-868,717Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv471332RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000005.10Chr5687,886815,602
nsv471332RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000005.9Chr5688,001815,717
nsv471332Submitted genomicNCBI35 (hg17)NC_000005.8Chr5741,001868,717

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv547993copy number gainJDWSequencingRead depth3198
nssv547994copy number gainNA18507SequencingRead depth5208
nssv547995copy number gainYHSequencingRead depth6201

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nssv547993RemappedPerfectNC_000005.10:g.(68
7886_?)_(?_815602)
dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000005.10Chr5687,886815,602
nssv547994RemappedPerfectNC_000005.10:g.(68
7886_?)_(?_815602)
dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000005.10Chr5687,886815,602
nssv547995RemappedPerfectNC_000005.10:g.(68
7886_?)_(?_815602)
dup
GRCh38 (hg38)Primary AssemblyFirst PassNC_000005.10Chr5687,886815,602
nssv547993RemappedPerfectNC_000005.9:g.(688
001_?)_(?_815717)d
up
GRCh37 (hg19)Primary AssemblyFirst PassNC_000005.9Chr5688,001815,717
nssv547994RemappedPerfectNC_000005.9:g.(688
001_?)_(?_815717)d
up
GRCh37 (hg19)Primary AssemblyFirst PassNC_000005.9Chr5688,001815,717
nssv547995RemappedPerfectNC_000005.9:g.(688
001_?)_(?_815717)d
up
GRCh37 (hg19)Primary AssemblyFirst PassNC_000005.9Chr5688,001815,717
nssv547993Submitted genomicNC_000005.8:g.(741
001_?)_(?_868717)d
up
NCBI35 (hg17)NC_000005.8Chr5741,001868,717
nssv547994Submitted genomicNC_000005.8:g.(741
001_?)_(?_868717)d
up
NCBI35 (hg17)NC_000005.8Chr5741,001868,717
nssv547995Submitted genomicNC_000005.8:g.(741
001_?)_(?_868717)d
up
NCBI35 (hg17)NC_000005.8Chr5741,001868,717

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
nssv5479933JDWOligo aCGHProbe signal intensityPass
nssv5479943NA18507Oligo aCGHProbe signal intensityPass
nssv5479953YHOligo aCGHProbe signal intensityPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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