A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901727



Internal ID15848997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54770165..54773045hg38UCSC Ensembl
Innerchr19:55281617..55284497hg19UCSC Ensembl
Innerchr19:59973429..59976309hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382881
hg192881
hg182881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580295
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)nssv901727
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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