A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646198



Internal ID7032943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56673046..56679740hg38UCSC Ensembl
chr20:55248102..55254796hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg386695
hg196695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv788e214
Supporting Variantsessv16218503, essv16218502, essv16218504
SamplesHG00732, HG00740, NA19080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646198
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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