A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6022600



Internal ID21931943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66496388..66496561hg38UCSC Ensembl
chr11:66263859..66264032hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590429
Samples
Known GenesDPP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6022600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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