A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645929



Internal ID7032676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45442074..45447750hg38UCSC Ensembl
Innerchr20:45442101..45447724hg38UCSC Ensembl
Outerchr20:45442048..45447777hg38UCSC Ensembl
chr20:44070714..44076390hg19UCSC Ensembl
Innerchr20:44070741..44076364hg19UCSC Ensembl
Outerchr20:44070688..44076417hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385677
hg195677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16196158
SamplesHG01951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645929
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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