A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052346



Internal ID21961580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18597987..18597987hg38UCSC Ensembl
chr1:18924481..18924481hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052346
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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