A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893927



Internal ID19184781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:60089282..60146135hg38UCSC Ensembl
Outerchr4:60089282..60146135hg38UCSC Ensembl
Innerchr4:60955000..61011853hg19UCSC Ensembl
Outerchr4:60955000..61011853hg19UCSC Ensembl
Innerchr4:60637595..60694448hg18UCSC Ensembl
Outerchr4:60637595..60694448hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3856854
hg1956854
hg1856854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787538
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893927
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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