A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615759



Internal ID21807806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122556752..122567124hg38UCSC Ensembl
chr12:123041299..123051671hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3810373
hg1910373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033288
Supporting Variants
Samples
Known GenesKNTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615759
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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