A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788826



Internal ID18818747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7418480..7876431hg38UCSC Ensembl
Innerchr8:7276002..7733953hg19UCSC Ensembl
Innerchr8:7263412..7771363hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38457952
hg19457952
hg18507952
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891321
Supporting Variants
Samples
Known GenesDEFB103A, DEFB103B, DEFB104A, DEFB104B, DEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B, FAM90A10P, FAM90A7P, PRR23D1, PRR23D2, SPAG11A, SPAG11B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788826
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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