A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526406



Internal ID21850764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171342733..171342733hg38UCSC Ensembl
chr1:171311872..171311872hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051578
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526406
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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