A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17395650



Internal ID22453520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23140060..23144418hg38UCSC Ensembl
chr20:23120697..23125055hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384359
hg194359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951319
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17395650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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