A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022152



Internal ID21931495
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 StatusM
Merged Variants
Supporting Variantsnssv17599227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022152
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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