A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645661



Internal ID6685723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32060998..32066402hg38UCSC Ensembl
Innerchr20:32061148..32066252hg38UCSC Ensembl
Outerchr20:32060848..32066552hg38UCSC Ensembl
chr20:30648801..30654205hg19UCSC Ensembl
Innerchr20:30648951..30654055hg19UCSC Ensembl
Outerchr20:30648651..30654355hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16173678
SamplesHG03472
Known GenesHCK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645661
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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