A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033312



Internal ID18775846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11269291..11394661hg38UCSC Ensembl
Innerchr8:11126800..11252170hg19UCSC Ensembl
Innerchr8:11164210..11289580hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38125371
hg19125371
hg18125371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3754238
Samples
Known GenesC8orf12, MTMR9, SLC35G5, TDH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033312
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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