A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109533



Internal ID21487767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158849970..158870969hg38UCSC Ensembl
chr2:159706482..159727481hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575038
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109533
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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