A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11357067



Internal ID377869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11369805..11379264hg38UCSC Ensembl
Innerchr4:11369805..11379264hg38UCSC Ensembl
Outerchr4:11369305..11379764hg38UCSC Ensembl
chr4:11371429..11380888hg19UCSC Ensembl
Innerchr4:11371429..11380888hg19UCSC Ensembl
Outerchr4:11370929..11381388hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg389460
hg199460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599644
Supporting Variants
SamplesHG00109
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11357067
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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