A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149350



Internal ID21445408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13882318..13883620hg38UCSC Ensembl
chr6:13882549..13883851hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381303
hg191303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571346
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149350
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