A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023972



Internal ID21933315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43979542..43990591hg38UCSC Ensembl
chr11:44001092..44012141hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3811050
hg1911050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023972
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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