A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075645



Internal ID21984878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34893473..34893473hg38UCSC Ensembl
chr3:34934965..34934965hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075645
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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