A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17403129



Internal ID22460999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168262330..168263683hg38UCSC Ensembl
chr2:169118840..169120193hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381354
hg191354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17403129
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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