A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526846



Internal ID21851203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189896183..189896183hg38UCSC Ensembl
chr2:190760909..190760909hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055414
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526846
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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