A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072432



Internal ID21981665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18594313..18594313hg38UCSC Ensembl
chr8:18451823..18451823hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563290
Samples
Known GenesPSD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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