A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506565



Internal ID20879847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38736563..38737641hg38UCSC Ensembl
chr17:36892816..36893894hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035296
Samples
Known GenesPCGF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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