A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606061



Internal ID21798108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50151339..50151339hg38UCSC Ensembl
chr12:50545122..50545122hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg382624
hg192624
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097222
Supporting Variants
Samples
Known GenesCERS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606061
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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