A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060991



Internal ID21970224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81062982..81062982hg38UCSC Ensembl
chr8:81975217..81975217hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595798
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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