A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488680



Internal ID22546597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94232721..94242503hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389783
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488680
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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