A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077179



Internal ID21986412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:55583455..55583455hg38UCSC Ensembl
chr3:55617483..55617483hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543839
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077179
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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