A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590367



Internal ID21538936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31042917..31043140hg38UCSC Ensembl
chr9:31042915..31043138hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161907
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590367
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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