A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891076



Internal ID18838786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16906862..17523278hg38UCSC Ensembl
Outerchr7:16794737..17707004hg38UCSC Ensembl
Innerchr7:16946486..17562902hg19UCSC Ensembl
Outerchr7:16834361..17746628hg19UCSC Ensembl
Innerchr7:16913011..17529427hg18UCSC Ensembl
Outerchr7:16800886..17713153hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38912268
hg19912268
hg18912268
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790455, essv25792234
Samples
Known GenesAGR2, AGR3, AHR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891076
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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