A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535554



Internal ID21859909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84553832..84553832hg38UCSC Ensembl
chr1:85019515..85019515hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040763
Supporting Variants
Samples
Known GenesCTBS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535554
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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