A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159066



Internal ID21510255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69515180..69515384hg38UCSC Ensembl
chr5:68811007..68811211hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564859
Supporting Variants
SamplesNA24385
Known GenesOCLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159066
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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