A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17625703



Internal ID21817750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67949026..67950831hg38UCSC Ensembl
chr17:65945142..65946947hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381806
hg191806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025648
Supporting Variants
Samples
Known GenesBPTF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17625703
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