A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135283



Internal ID21505868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186464229..186465323hg38UCSC Ensembl
chr3:186182018..186183112hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381095
hg191095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564748
Supporting Variants
SamplesNA19983
Known GenesLOC253573
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135283
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