A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17536563



Internal ID21860918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152160746..152160918hg38UCSC Ensembl
chr2:153017260..153017432hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5986503
Supporting Variants
Samples
Known GenesSTAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17536563
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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