A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790455



Internal ID18815015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16906862..17523278hg38UCSC Ensembl
Innerchr7:16946486..17562902hg19UCSC Ensembl
Innerchr7:16913011..17529427hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38616417
hg19616417
hg18616417
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891076
Supporting Variants
Samples
Known GenesAHR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=169
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790455
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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