A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073985



Internal ID21451287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32211766..32211837hg38UCSC Ensembl
chr11:32233312..32233383hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600330
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073985
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