A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891119



Internal ID19185515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61120915..62359499hg38UCSC Ensembl
Innerchr7:61103640..61803750hg19UCSC Ensembl
Outerchr7:61074140..62001639hg19UCSC Ensembl
Innerchr7:61107582..61441185hg18UCSC Ensembl
Outerchr7:61078082..61639074hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381238585
hg19927500
hg18560993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791268, essv25791621, essv25792242, essv25792070, essv25792406, essv25792065, essv25792072
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891119
Frequency
Sample Size3017
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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