A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036948



Internal ID21946291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50065205..50065380hg38UCSC Ensembl
chr13:50639341..50639516hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600453
Samples
Known GenesDLEU2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036948
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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