A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070413



Internal ID21979646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125067484..125067484hg38UCSC Ensembl
chr3:124786328..124786328hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070413
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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