A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008522



Internal ID19097740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:102796898..102932179hg38UCSC Ensembl
Innerchr3:102515742..102651023hg19UCSC Ensembl
Innerchr3:103998432..104133713hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38135282
hg19135282
hg18135282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604374
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)nsv1008522
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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