A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075792



Internal ID21498210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69534600..69534600hg38UCSC Ensembl
chr11:69349368..69349368hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663315
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075792
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer