A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797644



Internal ID19168581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7143522..7168834hg38UCSC Ensembl
Innerchr4:7145249..7170561hg19UCSC Ensembl
Innerchr4:7196150..7221462hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3825313
hg1925313
hg1825313
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893866
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=13
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797644
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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