A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179071



Internal ID20746111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39149035..39151988hg38UCSC Ensembl
chr17:37305288..37308241hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg382954
hg192954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503180
Supporting Variants
Samples
Known GenesPLXDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179071
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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