A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755566



Internal ID20531426
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 StatusM
Merged Variants
Supporting Variantsnssv16262512
Samples
Known GenesPOLB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755566
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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