A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402415



Internal ID22460285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157343182..157344516hg38UCSC Ensembl
chr2:158199694..158201028hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg381335
hg191335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903208
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402415
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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