A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023590



Internal ID21932933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60815390..60815569hg38UCSC Ensembl
chr11:60582863..60583042hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023590
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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