A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893903



Internal ID19184757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28641104..28722232hg38UCSC Ensembl
Outerchr4:28641104..28722232hg38UCSC Ensembl
Innerchr4:28642726..28723854hg19UCSC Ensembl
Outerchr4:28642726..28723854hg19UCSC Ensembl
Innerchr4:28251824..28332952hg18UCSC Ensembl
Outerchr4:28251824..28332952hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3881129
hg1981129
hg1881129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800362
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893903
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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