A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072835



Internal ID21982068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94110332..94110332hg38UCSC Ensembl
chr3:93829176..93829176hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551683
Samples
Known GenesNSUN3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072835
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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