A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790912



Internal ID19181321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4437381..4602171hg38UCSC Ensembl
Innerchr7:4477012..4641802hg19UCSC Ensembl
Innerchr7:4443538..4608328hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38164791
hg19164791
hg18164791
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891022
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=47
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790912
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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