A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084459



Internal ID21993692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119675776..119675776hg38UCSC Ensembl
chr10:121435288..121435288hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578568
Samples
Known GenesBAG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084459
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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