A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965828



Internal ID22740763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176687283..176687283hg38UCSC Ensembl
chr2:177552011..177552011hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965828
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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