A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891153



Internal ID19185549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:81176512..81608694hg38UCSC Ensembl
Outerchr7:81176512..81608694hg38UCSC Ensembl
Innerchr7:80805828..81238010hg19UCSC Ensembl
Outerchr7:80805828..81238010hg19UCSC Ensembl
Innerchr7:80643764..81075946hg18UCSC Ensembl
Outerchr7:80643764..81075946hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38432183
hg19432183
hg18432183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792655
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891153
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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