A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005321



Internal ID19094538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21840844..21864139hg38UCSC Ensembl
Innerchr3:21882336..21905631hg19UCSC Ensembl
Innerchr3:21857340..21880635hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3823296
hg1923296
hg1823296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593159
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005321
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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