A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036111



Internal ID21945454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50634241..50635441hg38UCSC Ensembl
chr13:51208377..51209577hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036111
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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