A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645816



Internal ID7032564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40003528..40014870hg38UCSC Ensembl
Innerchr20:40003678..40014720hg38UCSC Ensembl
Outerchr20:40003378..40015020hg38UCSC Ensembl
chr20:38632170..38643512hg19UCSC Ensembl
Innerchr20:38632320..38643362hg19UCSC Ensembl
Outerchr20:38632020..38643662hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3811343
hg1911343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16186547
SamplesHG02574
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645816
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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