A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568801



Internal ID21517152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235709445..235709955hg38UCSC Ensembl
chr1:235872745..235873255hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063600
SamplesHG03486
Known GenesLYST
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568801
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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