A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792065



Internal ID19173317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61110083..62359499hg38UCSC Ensembl
Innerchr7:61092808..61803750hg19UCSC Ensembl
Innerchr7:61096750..61441185hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381249417
hg19710943
hg18344436
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891119
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=69
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792065
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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