A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566737



Internal ID21758780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66344395..66345992hg38UCSC Ensembl
chr7:65809382..65810979hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381598
hg191598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014672
Supporting Variants
Samples
Known GenesTPST1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566737
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