A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109506



Internal ID21413263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15481512..15481610hg38UCSC Ensembl
chr2:15621636..15621734hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584032
Supporting Variants
SamplesHG00513
Known GenesNBAS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109506
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