A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901644



Internal ID15848914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54735664..54851404hg38UCSC Ensembl
Innerchr19:55247131..55362859hg19UCSC Ensembl
Innerchr19:59938943..60054671hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38115741
hg19115729
hg18115729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580248
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, KIR3DL3, LOC100287534
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901644
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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