A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074908



Internal ID21474974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38665238..38665543hg38UCSC Ensembl
chr11:38686788..38687093hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598770
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074908
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