A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783994



Internal ID19178022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160968831..161188535hg38UCSC Ensembl
Innerchr4:161889983..162109687hg19UCSC Ensembl
Innerchr4:162109433..162329137hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38219705
hg19219705
hg18219705
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894062
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=49
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783994
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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