A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17113573



Internal ID21467546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65930480..65933264hg38UCSC Ensembl
chr2:66157614..66160398hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382785
hg192785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582738
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17113573
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