A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952851



Internal ID22728155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170599447..170599447hg38UCSC Ensembl
chr1:170568588..170568588hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952851
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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