A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6021216



Internal ID21930559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129837502..129841685hg38UCSC Ensembl
chr11:129707397..129711580hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg384184
hg194184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605528
Samples
Known GenesTMEM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6021216
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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