A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800985



Internal ID19167869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:101501065..101562626hg38UCSC Ensembl
Innerchr4:102422222..102483783hg19UCSC Ensembl
Innerchr4:102641245..102702806hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3861562
hg1961562
hg1861562
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893998
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800985
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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