A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042480



Internal ID21951796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90005765..90005765hg38UCSC Ensembl
chr1:90471324..90471324hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519329
Samples
Known GenesZNF326
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042480
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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