A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580583



Internal ID21529075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206135429..206141439hg38UCSC Ensembl
chr1:206199891..206205901hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg386011
hg196011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062746
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580583
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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