A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481971



Internal ID22539876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199482120..199486056hg38UCSC Ensembl
chr2:200346843..200350779hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg383937
hg193937
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832361
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481971
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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