A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645902



Internal ID7032650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44076876..44077534hg38UCSC Ensembl
Innerchr20:44076926..44077484hg38UCSC Ensembl
Outerchr20:44076826..44077584hg38UCSC Ensembl
chr20:42705516..42706174hg19UCSC Ensembl
Innerchr20:42705566..42706124hg19UCSC Ensembl
Outerchr20:42705466..42706224hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16193784
SamplesNA20535
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645902
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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