A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893902



Internal ID19184756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:28242747..28622643hg38UCSC Ensembl
Outerchr4:28242747..28622643hg38UCSC Ensembl
Innerchr4:28244369..28624265hg19UCSC Ensembl
Outerchr4:28244369..28624265hg19UCSC Ensembl
Innerchr4:27853467..28233363hg18UCSC Ensembl
Outerchr4:27853467..28233363hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38379897
hg19379897
hg18379897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785961
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893902
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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