A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073262



Internal ID21502185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131633692..131633765hg38UCSC Ensembl
chr11:131503586..131503659hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587251
Supporting Variants
SamplesNA19239
Known GenesNTM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073262
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