A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029144



Internal ID21938487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117513273..117516074hg38UCSC Ensembl
chr11:117383988..117386789hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612144
Samples
Known GenesDSCAML1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029144
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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