A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799533



Internal ID18828617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:82211348..82297077hg38UCSC Ensembl
Innerchr4:83132501..83218230hg19UCSC Ensembl
Innerchr4:83351525..83437254hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3885730
hg1985730
hg1885730
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893970
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799533
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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