A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6935n100



Internal ID20158551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:7392846..7969833hg38UCSC Ensembl
chr8:7250368..7827355hg19UCSC Ensembl
chr8:7237778..7864765hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38576988
hg19576988
hg18626988
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032284, nsv1018311, nsv1027201, nsv1016808, nsv1031104, nsv1031015, nsv1020224, nsv1023775, nsv1030353, nsv1031910, nsv1026662, nsv1031031, nsv1022277, nsv1029956, nsv1025716, nsv1027941, nsv1034141, nsv1021592, nsv1033042, nsv1031330, nsv1031348, nsv1026637, nsv1033574, nsv1015704, nsv1027085, nsv1019709, nsv1020432, nsv1024605, nsv1030268, nsv1026917, nsv1019371, nsv1020827, nsv1031021, nsv1026365, nsv1019260, nsv1027951, nsv1025370, nsv1024589, nsv1024071, nsv1029520, nsv1021436, nsv1026945, nsv1019292, nsv1015189, nsv1030906, nsv1019662, nsv1024326, nsv1020998, nsv1016141, nsv1021960, nsv1016025, nsv1017982, nsv1026165, nsv1018094, nsv1029629, nsv1032668, nsv1031679, nsv1028394, nsv1027479, nsv1021549, nsv1031103, nsv1029643
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB4A, DEFB4B, FAM66E, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, ZNF705B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6935n100
Frequency
Sample Size29084
Observed Gain204
Observed Loss0
Observed Complex0
Frequencyn/a


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