A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792234



Internal ID18827700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16794737..17707004hg38UCSC Ensembl
Innerchr7:16834361..17746628hg19UCSC Ensembl
Innerchr7:16800886..17713153hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38912268
hg19912268
hg18912268
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891076
Supporting Variants
Samples
Known GenesAGR2, AGR3, AHR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=297
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792234
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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