A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079834



Internal ID21989067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5305009..5305009hg38UCSC Ensembl
chr5:5305122..5305122hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546869
Samples
Known GenesADAMTS16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079834
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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