A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074372



Internal ID21467678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35986025..35986025hg38UCSC Ensembl
chr11:36007575..36007575hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662321
Supporting Variants
SamplesHG03125
Known GenesLDLRAD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074372
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