A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602733



Internal ID6989766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153838150..153840143hg38UCSC Ensembl
Innerchr4:153838150..153840143hg38UCSC Ensembl
Outerchr4:153838114..153840253hg38UCSC Ensembl
chr4:154759302..154761295hg19UCSC Ensembl
Innerchr4:154759302..154761295hg19UCSC Ensembl
Outerchr4:154759266..154761405hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg381994
hg191994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11655882
SamplesNA20828
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602733
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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