A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590669



Internal ID21782712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54166679..54172065hg38UCSC Ensembl
chr10:55926439..55931825hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg385387
hg195387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010447
Supporting Variants
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590669
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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