A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537224



Internal ID21861579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215299941..215316769hg38UCSC Ensembl
chr2:216164664..216181492hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3816829
hg1916829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987535
Supporting Variants
Samples
Known GenesATIC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537224
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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