A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062889



Internal ID21972122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57304947..57304947hg38UCSC Ensembl
chr3:57338975..57338975hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546691
Samples
Known GenesDNAH12
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062889
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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