A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033589



Internal ID18776122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2490387..3447578hg38UCSC Ensembl
Innerchr8:2347503..3305100hg19UCSC Ensembl
Innerchr8:2334910..3292508hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38957192
hg19957598
hg18957599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675289
Samples
Known GenesCSMD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033589
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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