A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397143



Internal ID22455013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45437439..45441121hg38UCSC Ensembl
chr20:44066079..44069761hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg383683
hg193683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397143
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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