A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17399891



Internal ID22457761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119659503..119660911hg38UCSC Ensembl
chr2:120417079..120418487hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg381409
hg191409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897296
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17399891
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.05


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