A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034745



Internal ID18777278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:13524571..13670170hg38UCSC Ensembl
Innerchr8:13382080..13527679hg19UCSC Ensembl
Innerchr8:13426451..13572050hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38145600
hg19145600
hg18145600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760203
Samples
Known GenesC8orf48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034745
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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