A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017791



Internal ID19107008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:112941087..113005248hg38UCSC Ensembl
Innerchr8:113953316..114017477hg19UCSC Ensembl
Innerchr8:114022492..114086653hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3864162
hg1964162
hg1864162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691303
Samples
Known GenesCSMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017791
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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