A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580314



Internal ID16021037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54772775..54776372hg38UCSC Ensembl
Innerchr19:55284227..55287824hg19UCSC Ensembl
Innerchr19:59976039..59979636hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383598
hg193598
hg183598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6577n54
Supporting Variantsnssv901768
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580314
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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