A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452429



Internal ID21109982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91823397..91825168hg38UCSC Ensembl
chr10:93583154..93584925hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381772
hg191772
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184212
Samples
Known GenesTNKS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452429
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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