A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17633683



Internal ID21825730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28318809..28321562hg38UCSC Ensembl
chr17:26645835..26648588hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382754
hg192754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024599
Supporting Variants
Samples
Known GenesTMEM97
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17633683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer