A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891152



Internal ID19185548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80959400..80991081hg38UCSC Ensembl
Outerchr7:80959400..80991081hg38UCSC Ensembl
Innerchr7:80588716..80620397hg19UCSC Ensembl
Outerchr7:80588716..80620397hg19UCSC Ensembl
Innerchr7:80426652..80458333hg18UCSC Ensembl
Outerchr7:80426652..80458333hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3831682
hg1931682
hg1831682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783415
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891152
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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