A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580263



Internal ID16020986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54750252..54772775hg38UCSC Ensembl
Innerchr19:55261704..55284227hg19UCSC Ensembl
Innerchr19:59953516..59976039hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3822524
hg1922524
hg1822524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6566n54
Supporting Variantsnssv901673, nssv901672
Samples
Known GenesKIR2DL1, KIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580263
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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