A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052084



Internal ID21961317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149087170..149087170hg38UCSC Ensembl
chr1:148352108..148352108hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536462
Samples
Known GenesLOC101929780
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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