A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580255



Internal ID16020978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54748501..54771566hg38UCSC Ensembl
Innerchr19:55259953..55283018hg19UCSC Ensembl
Innerchr19:59951765..59974830hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3823066
hg1923066
hg1823066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901652
Samples
Known GenesKIR2DL1, KIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580255
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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