A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv6911n100

Internal ID20158527
Location Information
TypeCoordinatesAssemblyOther Links
chr8:7312955..8008628hg38UCSC Ensembl
chr8:7170477..7866150hg19UCSC Ensembl
chr8:7157887..7903560hg18UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035117, nsv1025822, nsv1018609, nsv1023807, nsv1021926, nsv1017678, nsv1022330, nsv1022600, nsv1023693, nsv1027154, nsv1024259, nsv1017159, nsv1021694, nsv1023863, nsv1021601, nsv1028744, nsv1026177, nsv1029692, nsv1025369, nsv1022535, nsv1023253, nsv1033901, nsv1030688, nsv1025377, nsv1018509, nsv1029299, nsv1022394, nsv1034348, nsv1020317, nsv1023895, nsv1021045, nsv1019660, nsv1018310, nsv1033999, nsv1032093, nsv1018350, nsv1029041, nsv1019482, nsv1027099, nsv1022960, nsv1017358, nsv1033307, nsv1034084, nsv1033969, nsv1027638, nsv1020164, nsv1024993, nsv1024672, nsv1021667, nsv1020878, nsv1033302, nsv1024941, nsv1019437, nsv1016964, nsv1015904, nsv1024870, nsv1015439, nsv1028169, nsv1034025, nsv1028464, nsv1035053, nsv1027579, nsv1033945, nsv1034627, nsv1031043, nsv1020392, nsv1034827, nsv1015281, nsv1032486, nsv1024952, nsv1016051, nsv1015869, nsv1032937, nsv1029829, nsv1025435, nsv1026625, nsv1032313, nsv1034290
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4A, DEFB4B, FAM66B, FAM66E, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L1P, USP17L3, USP17L4, USP17L8, ZNF705B, ZNF705G
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Pubmed ID25217958
Accession Number(s)dgv6911n100
Sample Size29084
Observed Gain0
Observed Loss113
Observed Complex0

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