A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033850



Internal ID21943193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30469463..30469687hg38UCSC Ensembl
chr13:31043600..31043824hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033850
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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