A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071790



Internal ID21981023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136714951..136714951hg38UCSC Ensembl
chr3:136433793..136433793hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544826
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071790
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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