A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607661



Internal ID20980732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162124663..162739694hg38UCSC Ensembl
chr6:162545695..163160726hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38615032
hg19615032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216756
Samples
Known GenesPACRG, PARK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607661
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer