A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580813



Internal ID21772856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32031868..32031868hg38UCSC Ensembl
chr10:32320796..32320796hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092342
Supporting Variants
Samples
Known GenesKIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580813
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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