A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520859



Internal ID21845218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:118155966..118155966hg38UCSC Ensembl
chr2:118913542..118913542hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052557
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520859
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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