A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074325



Internal ID21983558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127373244..127373244hg38UCSC Ensembl
chr3:127092087..127092087hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547094
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074325
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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