A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617465



Internal ID21809512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27062403..27062517hg38UCSC Ensembl
chr12:27215336..27215450hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035766
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617465
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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