A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889026



Internal ID22664037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165662127..165662176hg38UCSC Ensembl
chr2:166518637..166518686hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398158
Samples
Known GenesCSRNP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889026
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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