A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601439



Internal ID21793486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62409981..62421017hg38UCSC Ensembl
chr12:62803761..62814797hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3811037
hg1911037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601439
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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