A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020042



Internal ID21929385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94444898..94445008hg38UCSC Ensembl
chr10:96204655..96204765hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591605
Samples
Known GenesTBC1D12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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