A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17389755



Internal ID22447625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101943980..101955422hg38UCSC Ensembl
chr2:102560442..102571884hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3811443
hg1911443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884413
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17389755
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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