A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074466



Internal ID21452830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37588450..37588499hg38UCSC Ensembl
chr11:37610000..37610049hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601358
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074466
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