A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088060



Internal ID21491351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72236607..72236607hg38UCSC Ensembl
chr17:70232748..70232748hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655165
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088060
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