A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480611



Internal ID22538514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161613583..161615182hg38UCSC Ensembl
chr2:162470093..162471692hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480611
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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