A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032625



Internal ID21941968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112077172..112181466hg38UCSC Ensembl
chr11:111947896..112052189hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38104295
hg19104294
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601307
Samples
Known GenesBCO2, C11orf57, IL18, SDHD, TEX12, TIMM8B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032625
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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