A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646283



Internal ID7033028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61941788..61959104hg38UCSC Ensembl
Innerchr20:61941802..61959090hg38UCSC Ensembl
Outerchr20:61941774..61959118hg38UCSC Ensembl
chr20:60516844..60534160hg19UCSC Ensembl
Innerchr20:60516858..60534146hg19UCSC Ensembl
Outerchr20:60516830..60534174hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3817317
hg1917317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16220608, essv16220607
SamplesHG03235, HG03977
Known GenesMIR1257
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646283
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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