A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893910



Internal ID19184764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34108692..34180899hg38UCSC Ensembl
Outerchr4:34108410..34229433hg38UCSC Ensembl
Innerchr4:34110314..34182521hg19UCSC Ensembl
Outerchr4:34110032..34231055hg19UCSC Ensembl
Innerchr4:33786709..33858916hg18UCSC Ensembl
Outerchr4:33786427..33907450hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38121024
hg19121024
hg18121024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25801238, essv25796817
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893910
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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