A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515093



Internal ID18813374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:33666502..33723575hg38UCSC Ensembl
Innerchr10:33955430..34012503hg19UCSC Ensembl
Innerchr10:33995436..34052509hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3857074
hg1957074
hg1857074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052653
Supporting Variants
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)nssv3515093
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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