A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901755



Internal ID15849025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54772261..54774689hg38UCSC Ensembl
Innerchr19:55283713..55286141hg19UCSC Ensembl
Innerchr19:59975525..59977953hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382429
hg192429
hg182429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580307
Supporting Variants
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901755
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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