A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075301



Internal ID21484685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66837701..66841371hg38UCSC Ensembl
chr11:66605172..66608842hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg383671
hg193671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601195
Supporting Variants
SamplesNA12329
Known GenesC11orf80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075301
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