A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611270



Internal ID21803317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17448762..17460642hg38UCSC Ensembl
chr12:17601696..17613576hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3811881
hg1911881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611270
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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