A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783577



Internal ID19176211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120278315..120484900hg38UCSC Ensembl
Innerchr4:121199470..121406055hg19UCSC Ensembl
Innerchr4:121418920..121625505hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38206586
hg19206586
hg18206586
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894017
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783577
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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