A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645703



Internal ID6685765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34618369..34622782hg38UCSC Ensembl
Innerchr20:34618387..34622765hg38UCSC Ensembl
Outerchr20:34618352..34622800hg38UCSC Ensembl
chr20:33206173..33210586hg19UCSC Ensembl
Innerchr20:33206191..33210569hg19UCSC Ensembl
Outerchr20:33206156..33210604hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg384414
hg194414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16176722
SamplesHG01459
Known GenesPIGU
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645703
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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