A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077097



Internal ID21502794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107173452..107173452hg38UCSC Ensembl
chr12:107567230..107567230hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5650361
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077097
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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