A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791586



Internal ID18819733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7167337..7925394hg38UCSC Ensembl
Innerchr8:7024859..7782916hg19UCSC Ensembl
Innerchr8:7012269..7820326hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38758058
hg19758058
hg18808058
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, FAM90A10P, FAM90A7P, LINC00965, PRR23D1, PRR23D2, SPAG11A, SPAG11B, USP17L1P, USP17L4, ZNF705G
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=80
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791586
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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