A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000022



Internal ID21909365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5305007..5305129hg38UCSC Ensembl
chr5:5305120..5305242hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550507
Samples
Known GenesADAMTS16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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