A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015328



Internal ID21924671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17289530..17294742hg38UCSC Ensembl
chr10:17331529..17336741hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385213
hg195213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015328
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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