A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17630210



Internal ID21822257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55325530..55325530hg38UCSC Ensembl
chr16:55359442..55359442hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094162
Supporting Variants
Samples
Known GenesIRX6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17630210
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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