A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033792



Internal ID19123013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110812307..110894635hg38UCSC Ensembl
Innerchr8:111824536..111906864hg19UCSC Ensembl
Innerchr8:111893712..111976040hg18UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3882329
hg1982329
hg1882329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691284
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)nsv1033792
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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