A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073180



Internal ID21982413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120706613..120706613hg38UCSC Ensembl
chr3:120425460..120425460hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554124
Samples
Known GenesRABL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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