A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524690



Internal ID21849048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160813778..160813778hg38UCSC Ensembl
chr2:161670289..161670289hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524690
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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