A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894062



Internal ID19184916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160968831..161188535hg38UCSC Ensembl
Outerchr4:160968831..161188535hg38UCSC Ensembl
Innerchr4:161889983..162109687hg19UCSC Ensembl
Outerchr4:161889983..162109687hg19UCSC Ensembl
Innerchr4:162109433..162329137hg18UCSC Ensembl
Outerchr4:162109433..162329137hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38219705
hg19219705
hg18219705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783994
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894062
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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