A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv788e214



Internal ID22756682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56672739..56679740hg38UCSC Ensembl
chr20:55247795..55254796hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg387002
hg197002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3646197, esv3646198
SamplesHG00732, HG00740, NA19080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv788e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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