A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17102969



Internal ID21458374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79684903..79684903hg38UCSC Ensembl
chr18:77444903..77444903hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649373
Supporting Variants
SamplesHG02587
Known GenesCTDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17102969
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