A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079180



Internal ID21988413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3237101..3237101hg38UCSC Ensembl
chr6:3237335..3237335hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383810
hg193810
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079180
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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