A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521382



Internal ID20894743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34100424..34100980hg38UCSC Ensembl
chr20:32688230..32688786hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067478
Samples
Known GenesEIF2S2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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