A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087828



Internal ID21997061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32034560..32034560hg38UCSC Ensembl
chr10:32323488..32323488hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585905
Samples
Known GenesKIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087828
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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