A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17153463



Internal ID21512085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161646345..161646345hg38UCSC Ensembl
chr6:162067377..162067377hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636868
Supporting Variants
SamplesNA24385
Known GenesPARK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17153463
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