A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097773



Internal ID21463113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67838079..67838159hg38UCSC Ensembl
chr15:68130417..68130497hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586010
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097773
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