A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612199



Internal ID21804246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50135181..50135316hg38UCSC Ensembl
chr12:50528964..50529099hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6028886
Supporting Variants
Samples
Known GenesCERS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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