A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580284



Internal ID16021007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54764062..54782877hg38UCSC Ensembl
Innerchr19:55275514..55294329hg19UCSC Ensembl
Innerchr19:59967326..59986141hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3818816
hg1918816
hg1818816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901700
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580284
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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