A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149697



Internal ID21485327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163603793..163603793hg38UCSC Ensembl
chr6:164024825..164024825hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637399
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149697
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