A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614254



Internal ID21806301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98821785..98826947hg38UCSC Ensembl
chr12:99215563..99220725hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026204
Supporting Variants
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614254
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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