A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068972



Internal ID21978205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163321366..163321366hg38UCSC Ensembl
chr6:163742398..163742398hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569398
Samples
Known GenesPACRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068972
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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