A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580278



Internal ID16021001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54755753..54774689hg38UCSC Ensembl
Innerchr19:55267205..55286141hg19UCSC Ensembl
Innerchr19:59959017..59977953hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3818937
hg1918937
hg1818937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6568n54
Supporting Variantsnssv901693
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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