A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026283



Internal ID20593323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68939701..68941300hg38UCSC Ensembl
chr15:69232040..69233639hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513738
Supporting Variants
Samples
Known GenesMIR548H4, NOX5, SPESP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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