A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084926



Internal ID21994159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52561143..52561143hg38UCSC Ensembl
chr10:54320903..54320903hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084926
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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