A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986503



Internal ID21895846
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 StatusM
Merged Variants
Supporting Variantsnssv17536563
Samples
Known GenesSTAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986503
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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