A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17406452



Internal ID22464322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32739555..32740226hg38UCSC Ensembl
chr20:31327362..31328033hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963548
Supporting Variants
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17406452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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