A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783993



Internal ID19163338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160897056..160957840hg38UCSC Ensembl
Innerchr4:161818208..161878992hg19UCSC Ensembl
Innerchr4:162037658..162098442hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3860785
hg1960785
hg1860785
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894059
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783993
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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