A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963085



Internal ID22738020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37683604..37683899hg38UCSC Ensembl
chr20:36312006..36312301hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963085
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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