A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613342



Internal ID21805389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99477021..99477084hg38UCSC Ensembl
chr13:100129275..100129338hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613342
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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