A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068919



Internal ID21978152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56719992..56719992hg38UCSC Ensembl
chr3:56754020..56754020hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068919
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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