A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591638



Internal ID16379047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128690837..128713765hg38UCSC Ensembl
Innerchr3:128409680..128432608hg19UCSC Ensembl
Innerchr3:129892370..129915298hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3822929
hg1922929
hg1822929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973053
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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