A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5573920



Internal ID21522329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221151793..221153006hg38UCSC Ensembl
chr1:221325135..221326348hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381214
hg191214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063399
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5573920
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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