A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645138



Internal ID7031889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7526485..7530178hg38UCSC Ensembl
Innerchr20:7526485..7530178hg38UCSC Ensembl
Outerchr20:7526374..7530317hg38UCSC Ensembl
chr20:7507132..7510825hg19UCSC Ensembl
Innerchr20:7507132..7510825hg19UCSC Ensembl
Outerchr20:7507021..7510964hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg383694
hg193694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16133323
SamplesHG02076
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645138
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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