A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034823



Internal ID20601863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19648004..19660560hg38UCSC Ensembl
chr17:19551317..19563873hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3812557
hg1912557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513171
Supporting Variants
Samples
Known GenesALDH3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034823
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