A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097834



Internal ID22007067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82831525..82831525hg38UCSC Ensembl
chr11:82542567..82542567hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581623
Samples
Known GenesPRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097834
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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