A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037178



Internal ID21946521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63986719..63986816hg38UCSC Ensembl
chr11:63754191..63754288hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594501
Samples
Known GenesOTUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037178
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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