A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073717



Internal ID21982950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98837672..98837672hg38UCSC Ensembl
chr3:98556516..98556516hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546651
Samples
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073717
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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