A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155446



Internal ID21486339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82897764..82897764hg38UCSC Ensembl
chr6:83607483..83607483hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634953
Supporting Variants
SamplesNA12878
Known GenesUBE3D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155446
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