A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033684



Internal ID20600724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11272361..11278119hg38UCSC Ensembl
chr17:11175678..11181436hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385759
hg195759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512338
Supporting Variants
Samples
Known GenesSHISA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033684
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