A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392367



Internal ID22450237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31591567..31591567hg38UCSC Ensembl
chr21:32963880..32963880hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973149
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392367
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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