A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072681



Internal ID21981914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176326362..176326362hg38UCSC Ensembl
chr3:176044150..176044150hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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