A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010472



Internal ID19099689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21209827..21299371hg38UCSC Ensembl
Innerchr3:21251319..21340863hg19UCSC Ensembl
Innerchr3:21226323..21315867hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3889545
hg1989545
hg1889545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4690n100
Supporting Variantsnssv3739644
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)nsv1010472
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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