A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645548



Internal ID7032297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24321639..24322404hg38UCSC Ensembl
Innerchr20:24321645..24322399hg38UCSC Ensembl
Outerchr20:24321634..24322410hg38UCSC Ensembl
chr20:24302275..24303040hg19UCSC Ensembl
Innerchr20:24302281..24303035hg19UCSC Ensembl
Outerchr20:24302270..24303046hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38766
hg19766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163918
SamplesNA18536
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645548
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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