A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580313



Internal ID16021036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54772775..54776074hg38UCSC Ensembl
Innerchr19:55284227..55287526hg19UCSC Ensembl
Innerchr19:59976039..59979338hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383300
hg193300
hg183300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6577n54
Supporting Variantsnssv901767, nssv901766
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580313
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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