A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580315



Internal ID16021038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54772775..54778505hg38UCSC Ensembl
Innerchr19:55284227..55289957hg19UCSC Ensembl
Innerchr19:59976039..59981769hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg385731
hg195731
hg185731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901769
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580315
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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