A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894059



Internal ID19184913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160897056..160957840hg38UCSC Ensembl
Outerchr4:160897056..160957840hg38UCSC Ensembl
Innerchr4:161818208..161878992hg19UCSC Ensembl
Outerchr4:161818208..161878992hg19UCSC Ensembl
Innerchr4:162037658..162098442hg18UCSC Ensembl
Outerchr4:162037658..162098442hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3860785
hg1960785
hg1860785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783993
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894059
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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