A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401417



Internal ID22459287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33653671..33654761hg38UCSC Ensembl
chr20:32241477..32242567hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401417
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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