A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033319



Internal ID19122541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20749081..20860867hg38UCSC Ensembl
Innerchr8:20606592..20718378hg19UCSC Ensembl
Innerchr8:20650872..20762658hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38111787
hg19111787
hg18111787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685333
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)nsv1033319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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