A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17379647



Internal ID22437517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32928768..32928939hg38UCSC Ensembl
chr17:31255786..31255957hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936695
Supporting Variants
Samples
Known GenesTMEM98
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17379647
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