A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032782



Internal ID19122004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2473547..2738156hg38UCSC Ensembl
Innerchr8:2330755..2595684hg19UCSC Ensembl
Innerchr8:2318162..2583091hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38264610
hg19264930
hg18264930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6820n100
Supporting Variantsnssv3675281
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)nsv1032782
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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