A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012356



Internal ID21921699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96415717..96415774hg38UCSC Ensembl
chr10:98175474..98175531hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577929
Samples
Known GenesTLL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012356
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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