A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018185



Internal ID21927528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6629586..6635102hg38UCSC Ensembl
chr10:6671548..6677064hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385517
hg195517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018185
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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