A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505583



Internal ID20878854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17953032..17956320hg38UCSC Ensembl
chr17:17856346..17859634hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383289
hg193289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034111
Samples
Known GenesTOM1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505583
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