A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16232467



Internal ID4204656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63794884..63802781hg38UCSC Ensembl
Innerchr20:63794896..63802769hg38UCSC Ensembl
Outerchr20:63794872..63802793hg38UCSC Ensembl
chr20:62426237..62434134hg19UCSC Ensembl
Innerchr20:62426249..62434122hg19UCSC Ensembl
Outerchr20:62426225..62434146hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387898
hg197898
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646327
Supporting Variants
SamplesHG03787
Known GenesZBTB46
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16232467
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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