A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646197



Internal ID7032942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56672739..56679602hg38UCSC Ensembl
Innerchr20:56672789..56679534hg38UCSC Ensembl
Outerchr20:56672633..56679708hg38UCSC Ensembl
chr20:55247795..55254658hg19UCSC Ensembl
Innerchr20:55247845..55254590hg19UCSC Ensembl
Outerchr20:55247689..55254764hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg386864
hg196864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv788e214
Supporting Variantsessv16218501, essv16218500
SamplesHG00732, HG00740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646197
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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