A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020709



Internal ID18763244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2486412..2910610hg38UCSC Ensembl
Innerchr8:2343518..2768132hg19UCSC Ensembl
Innerchr8:2330925..2755539hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38424199
hg19424615
hg18424615
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6827n100
Supporting Variantsnssv3675287
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)nsv1020709
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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