A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797991



Internal ID19168381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138679151..138691439hg38UCSC Ensembl
Innerchr7:138363896..138376184hg19UCSC Ensembl
Innerchr7:138014436..138026724hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3812289
hg1912289
hg1812289
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891210
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797991
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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