A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16175672



Internal ID2739841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33698903..33701182hg38UCSC Ensembl
Innerchr20:33698953..33700867hg38UCSC Ensembl
Outerchr20:33698747..33701338hg38UCSC Ensembl
chr20:32286709..32288988hg19UCSC Ensembl
Innerchr20:32286759..32288673hg19UCSC Ensembl
Outerchr20:32286553..32289144hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382280
hg192280
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645687
Supporting Variants
SamplesHG02407
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16175672
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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