A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006411



Internal ID21915754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24988664..24988716hg38UCSC Ensembl
chr10:25277593..25277645hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578725
Samples
Known GenesENKUR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006411
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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