A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536736



Internal ID21861091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191667893..191667893hg38UCSC Ensembl
chr2:192532619..192532619hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040902
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536736
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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