A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033118



Internal ID21942461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13750351..13759261hg38UCSC Ensembl
chr11:13771898..13780808hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg388911
hg198911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033118
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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