A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607931



Internal ID21799978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69462259..69462585hg38UCSC Ensembl
chr13:70036391..70036717hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607931
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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