A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058402



Internal ID21967636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10002293..10002293hg38UCSC Ensembl
chr3:10043977..10043977hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531269
Samples
Known GenesEMC3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058402
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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