A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085763



Internal ID21511335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45969502..45969604hg38UCSC Ensembl
chr17:44046868..44046970hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598124
Supporting Variants
SamplesNA24385
Known GenesMAPT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085763
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