A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11655882



Internal ID6704077
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602733
Supporting Variants
SamplesNA20828
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11655882
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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