A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060691



Internal ID21969924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194311184..194311184hg38UCSC Ensembl
chr3:194028973..194028973hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539350
Samples
Known GenesLINC00887
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060691
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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