A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488809



Internal ID22546726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189546009..189554790hg38UCSC Ensembl
chr2:190410735..190419516hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg388782
hg198782
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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