A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17613341



Internal ID21805388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119360346..119360399hg38UCSC Ensembl
chr12:119798151..119798204hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037764
Supporting Variants
Samples
Known GenesCCDC60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17613341
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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