A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951420



Internal ID22726782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177561336..177561336hg38UCSC Ensembl
chr3:177279124..177279124hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422281
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951420
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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