A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959824



Internal ID22734843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19769885..19769885hg38UCSC Ensembl
chr1:20096378..20096378hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354538
Samples
Known GenesTMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959824
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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