A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598604



Internal ID21790649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10157540..10165274hg38UCSC Ensembl
chr12:10310139..10317873hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg387735
hg197735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027647
Supporting Variants
Samples
Known GenesOLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598604
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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