A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579958



Internal ID21528443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13558066..13575933hg38UCSC Ensembl
chr1:13884561..13902428hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3817868
hg1917868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060482
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579958
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