A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613094



Internal ID21805141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113954946..113955013hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024209
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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