A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262512



Internal ID20471730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42347292..42347292hg38UCSC Ensembl
chr8:42204810..42204810hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755566
Supporting Variants
Samples
Known GenesPOLB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262512
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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