A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027584



Internal ID19116803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77627587..77893901hg38UCSC Ensembl
Innerchr8:78539823..78806136hg19UCSC Ensembl
Innerchr8:78702378..78968691hg18UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38266315
hg19266314
hg18266314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689578
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)nsv1027584
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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