A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11641077



Internal ID3431135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145189111..145192333hg38UCSC Ensembl
Innerchr4:145189157..145192288hg38UCSC Ensembl
Outerchr4:145189066..145192379hg38UCSC Ensembl
chr4:146110263..146113485hg19UCSC Ensembl
Innerchr4:146110309..146113440hg19UCSC Ensembl
Outerchr4:146110218..146113531hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg383223
hg193223
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602556
Supporting Variants
SamplesHG03064
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11641077
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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