A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646191



Internal ID6686250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56431805..56436322hg38UCSC Ensembl
Innerchr20:56431848..56436280hg38UCSC Ensembl
Outerchr20:56431763..56436365hg38UCSC Ensembl
chr20:55006861..55011378hg19UCSC Ensembl
Innerchr20:55006904..55011336hg19UCSC Ensembl
Outerchr20:55006819..55011421hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16215930
SamplesHG03779
Known GenesCASS4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646191
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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