A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526282



Internal ID20899643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64524172..64528426hg38UCSC Ensembl
chr17:62520290..62524544hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg384255
hg194255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037792
Samples
Known GenesCEP95
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526282
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