A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075382



Internal ID21479738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57403440..57403531hg38UCSC Ensembl
chr11:57170913..57171004hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592010
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075382
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