A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891038



Internal ID19185434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7767046..7867221hg38UCSC Ensembl
Outerchr7:7767046..7867221hg38UCSC Ensembl
Innerchr7:7806677..7906852hg19UCSC Ensembl
Outerchr7:7806677..7906852hg19UCSC Ensembl
Innerchr7:7773202..7873377hg18UCSC Ensembl
Outerchr7:7773202..7873377hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38100176
hg19100176
hg18100176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788025
Samples
Known GenesRPA3-AS1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891038
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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