A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590852



Internal ID16378261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84629932..84678747hg38UCSC Ensembl
Innerchr3:84679083..84727898hg19UCSC Ensembl
Innerchr3:84761773..84810588hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3848816
hg1948816
hg1848816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967326
Samples
Known GenesLINC00971
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590852
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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