A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558459



Internal ID21882814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42233532..42233532hg38UCSC Ensembl
chr6:42201270..42201270hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073912
Supporting Variants
Samples
Known GenesTRERF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558459
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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