A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014491



Internal ID19103709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21209827..21315784hg38UCSC Ensembl
Innerchr3:21251319..21357276hg19UCSC Ensembl
Innerchr3:21226323..21332280hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38105958
hg19105958
hg18105958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4690n100
Supporting Variantsnssv3593120
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)nsv1014491
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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