A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599227



Internal ID21791272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48056208..48073113hg38UCSC Ensembl
chr13:48630344..48647249hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3816906
hg1916906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022152
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599227
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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