A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578101



Internal ID21526564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23993614..23993987hg38UCSC Ensembl
chr1:24320104..24320477hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17064185
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578101
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