A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779651



Internal ID19173036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120611403..120686461hg38UCSC Ensembl
Innerchr4:121532558..121607616hg19UCSC Ensembl
Innerchr4:121752008..121827066hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3875059
hg1975059
hg1875059
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894018
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779651
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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