A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015573



Internal ID21924916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:217860..639697hg38UCSC Ensembl
chr10:263800..685637hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38421838
hg19421838
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587610
Samples
Known GenesDIP2C, ZMYND11
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015573
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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