A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891077



Internal ID18838787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17172449..17590374hg38UCSC Ensembl
Outerchr7:17172449..17590374hg38UCSC Ensembl
Innerchr7:17212073..17629998hg19UCSC Ensembl
Outerchr7:17212073..17629998hg19UCSC Ensembl
Innerchr7:17178598..17596523hg18UCSC Ensembl
Outerchr7:17178598..17596523hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38417926
hg19417926
hg18417926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789932
Samples
Known GenesAHR
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891077
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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