A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797954



Internal ID19178957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148628234..148660487hg38UCSC Ensembl
Innerchr7:148325326..148357579hg19UCSC Ensembl
Innerchr7:147956259..147988512hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3832254
hg1932254
hg1832254
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891232
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797954
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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