A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033718



Internal ID21943061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76933185..76933530hg38UCSC Ensembl
chr11:76644229..76644574hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586858
Samples
Known GenesACER3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033718
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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