A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788265



Internal ID19165873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:48800799..48838524hg38UCSC Ensembl
Innerchr7:48840395..48878120hg19UCSC Ensembl
Innerchr7:48810941..48848666hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3837726
hg1937726
hg1837726
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891107
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788265
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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