A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589623



Internal ID16377032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779054..8816277hg38UCSC Ensembl
Innerchr3:8820740..8857963hg19UCSC Ensembl
Innerchr3:8795740..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837224
hg1937224
hg1837224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8214n54
Supporting Variantsnssv1151842
Samples1780862578_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589623
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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