A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635349



Internal ID21583654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161646536..161646536hg38UCSC Ensembl
chr6:162067568..162067568hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145545
SamplesHG03486
Known GenesPARK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635349
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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