A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036191



Internal ID21945534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49819112..49819198hg38UCSC Ensembl
chr13:50393248..50393334hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036191
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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