A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036510



Internal ID20603550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:59860001..59862700hg38UCSC Ensembl
chr17:57937362..57940061hg19UCSC Ensembl
Cytoband17q23.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528668
Supporting Variants
Samples
Known GenesTUBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036510
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