A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787855



Internal ID19181282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54055558..54110080hg38UCSC Ensembl
Innerchr7:54123251..54177773hg19UCSC Ensembl
Innerchr7:54090745..54145267hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3854523
hg1954523
hg1854523
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891112
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787855
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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