A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953961



Internal ID21374030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63559526..63559786hg38UCSC Ensembl
chr20:62190879..62191139hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15178128
SamplesHG002
Known GenesHELZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953961
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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