A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579544



Internal ID21771587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42347394..42347394hg38UCSC Ensembl
chr8:42204912..42204912hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066818
Supporting Variants
Samples
Known GenesPOLB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579544
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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