A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590988



Internal ID16378397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:94665488..94877228hg38UCSC Ensembl
Innerchr3:94384332..94596072hg19UCSC Ensembl
Innerchr3:95867022..96078762hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38211741
hg19211741
hg18211741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152501
Samples1780862081_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590988
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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