A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568719



Internal ID21517068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152286700..152293598hg38UCSC Ensembl
chr5:151666261..151673159hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg386899
hg196899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125256
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568719
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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