A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617527



Internal ID21809574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102576219..102576219hg38UCSC Ensembl
chr12:102969997..102969997hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6081494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617527
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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