A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003152



Internal ID19092369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90208672..90436800hg38UCSC Ensembl
Innerchr3:90257822..90485950hg19UCSC Ensembl
Innerchr3:90340512..90568640hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38228129
hg19228129
hg18228129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4812n100
Supporting Variantsnssv3603282
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)nsv1003152
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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