A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6958n100



Internal ID20158574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:7775544..7896858hg38UCSC Ensembl
chr8:7633066..7754380hg19UCSC Ensembl
chr8:7670476..7791790hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38121315
hg19121315
hg18121315
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033118, nsv1025194
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, PRR23D1, PRR23D2, SPAG11A, SPAG11B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6958n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss6
Observed Complex0
Frequencyn/a


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