A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580305



Internal ID16021028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54771566..54775343hg38UCSC Ensembl
Innerchr19:55283018..55286795hg19UCSC Ensembl
Innerchr19:59974830..59978607hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383778
hg193778
hg183778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901751
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580305
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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