A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17126710



Internal ID21453782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170237234..170454415hg38UCSC Ensembl
chr4:171158385..171375566hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38217182
hg19217182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573445
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17126710
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