A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071341



Internal ID21490299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80482350..80482798hg38UCSC Ensembl
chr10:82242106..82242554hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590635
Supporting Variants
SamplesNA19238
Known GenesTSPAN14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071341
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