A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602462



Internal ID21794509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102405254..102405254hg38UCSC Ensembl
chr12:102799032..102799032hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090414
Supporting Variants
Samples
Known GenesIGF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602462
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer