A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615557



Internal ID21807604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122277259..122288979hg38UCSC Ensembl
chr12:122761806..122773526hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3811721
hg1911721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6021806
Supporting Variants
Samples
Known GenesCLIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615557
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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