A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061726



Internal ID21970959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171969737..171969737hg38UCSC Ensembl
chr3:171687527..171687527hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061726
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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