A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034263



Internal ID18776797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7433385..7541457hg38UCSC Ensembl
Innerchr8:7290907..7398979hg19UCSC Ensembl
Innerchr8:7278317..7386389hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38108073
hg19108073
hg18108073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6942n100
Supporting Variantsnssv3680177, nssv3680178
Samples
Known GenesDEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, PRR23D1, PRR23D2, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034263
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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