A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038448



Internal ID21947791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132744937..132744991hg38UCSC Ensembl
chr11:132614832..132614886hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611719
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038448
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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