A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529190



Internal ID21853547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220744116..220744116hg38UCSC Ensembl
chr2:221608836..221608836hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529190
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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