A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099882



Internal ID22009115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32132250..32132250hg38UCSC Ensembl
chr13:32706387..32706387hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599240
Samples
Known GenesFRY
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099882
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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