A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617448



Internal ID21809495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10225136..10225287hg38UCSC Ensembl
chr12:10377735..10377886hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617448
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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