A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791297



Internal ID18814509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7204888..7959791hg38UCSC Ensembl
Innerchr8:7062410..7817313hg19UCSC Ensembl
Innerchr8:7049820..7854723hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38754904
hg19754904
hg18804904
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891318
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, DEFB109P1B, DEFB4A, DEFB4B, FAM66B, FAM66E, FAM90A10P, FAM90A7P, LINC00965, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L1P, USP17L4, ZNF705B, ZNF705G
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=85
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791297
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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