A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893885



Internal ID18838019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15777609..15887721hg38UCSC Ensembl
Outerchr4:15777609..15887721hg38UCSC Ensembl
Innerchr4:15779232..15889344hg19UCSC Ensembl
Outerchr4:15779232..15889344hg19UCSC Ensembl
Innerchr4:15388330..15498442hg18UCSC Ensembl
Outerchr4:15388330..15498442hg18UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38110113
hg19110113
hg18110113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798445
Samples
Known GenesCD38
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893885
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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