A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070682



Internal ID21979915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129516708..129516708hg38UCSC Ensembl
chr3:129235551..129235551hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551337
Samples
Known GenesIFT122
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070682
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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