A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034826



Internal ID20601866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19679701..19714800hg38UCSC Ensembl
chr17:19583014..19618113hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3835100
hg1935100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502863
Supporting Variants
Samples
Known GenesSLC47A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034826
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