A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610986



Internal ID21803033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55566540..55589944hg38UCSC Ensembl
chr12:55960324..55983728hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3823405
hg1923405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6039733
Supporting Variants
Samples
Known GenesOR2AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610986
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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