A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036571



Internal ID20603611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60780569..61046543hg38UCSC Ensembl
chr17:58857930..59123904hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38265975
hg19265975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529646
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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