A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591276



Internal ID16378685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111103649..111135349hg38UCSC Ensembl
Innerchr3:110822496..110854196hg19UCSC Ensembl
Innerchr3:112305186..112336886hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3831701
hg1931701
hg1831701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv971493
Samples
Known GenesPVRL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591276
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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