A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373721



Internal ID22599390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28692261..28692937hg38UCSC Ensembl
chr17:27019279..27019955hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934935
Supporting Variants
Samples
Known GenesSUPT6H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373721
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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