A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085983



Internal ID21995216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16260586..16260586hg38UCSC Ensembl
chr10:16302585..16302585hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085983
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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