A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645961



Internal ID7032707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46803873..46810445hg38UCSC Ensembl
Innerchr20:46803873..46810445hg38UCSC Ensembl
Outerchr20:46803373..46810945hg38UCSC Ensembl
chr20:45432512..45439084hg19UCSC Ensembl
Innerchr20:45432512..45439084hg19UCSC Ensembl
Outerchr20:45432012..45439584hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386573
hg196573
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16196823
SamplesHG02484
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645961
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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