A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580310



Internal ID16021033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54772261..54776372hg38UCSC Ensembl
Innerchr19:55283713..55287824hg19UCSC Ensembl
Innerchr19:59975525..59979636hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg384112
hg194112
hg184112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901762
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580310
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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