A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070601



Internal ID21979834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189312180..189312180hg38UCSC Ensembl
chr3:189029969..189029969hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539440
Samples
Known GenesTPRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070601
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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