A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162593



Internal ID21403692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67325252..67325653hg38UCSC Ensembl
chr9:47267349..47267750hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591503
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162593
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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