A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16213334



Internal ID4075723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56049529..56143244hg38UCSC Ensembl
chr20:54624585..54718300hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3893716
hg1993716
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646179
Supporting Variants
SamplesHG03708
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16213334
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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