A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136189



Internal ID21475655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26644925..26645006hg38UCSC Ensembl
chr4:26646547..26646628hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573875
Supporting Variants
SamplesHG03486
Known GenesTBC1D19
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136189
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