A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766165



Internal ID20542025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80911922..80911922hg38UCSC Ensembl
chr15:81204263..81204263hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269435
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766165
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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