A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893877



Internal ID18838011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10411544..10500710hg38UCSC Ensembl
Outerchr4:10411544..10500710hg38UCSC Ensembl
Innerchr4:10413168..10502334hg19UCSC Ensembl
Outerchr4:10413168..10502334hg19UCSC Ensembl
Innerchr4:10022266..10111432hg18UCSC Ensembl
Outerchr4:10022266..10111432hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3889167
hg1989167
hg1889167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796358
Samples
Known GenesCLNK, ZNF518B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893877
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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