A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016166



Internal ID21925509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23420967..23422732hg38UCSC Ensembl
chr10:23709896..23711661hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg381766
hg191766
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016166
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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