A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602967



Internal ID21795014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48331683..48334597hg38UCSC Ensembl
chr12:48725466..48728380hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg382915
hg192915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6034401
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602967
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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