A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703944



Internal ID127610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69176175..69176272hg38UCSC Ensembl
chr15:69468514..69468611hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529368
Supporting Variants
Samples
Known GenesGLCE, MIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703944
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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