A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026196



Internal ID18768728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7409831..8000485hg38UCSC Ensembl
Innerchr8:7267353..7858007hg19UCSC Ensembl
Innerchr8:7254763..7895417hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38590655
hg19590655
hg18640655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6909n100
Supporting Variantsnssv3680037
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4A, DEFB4B, FAM66E, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L3, USP17L8, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026196
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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