A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488266



Internal ID22546183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161067582..161068781hg38UCSC Ensembl
chr2:161924093..161925292hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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