A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568050



Internal ID21516394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81886660..81887001hg38UCSC Ensembl
chr5:81182479..81182820hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141447
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568050
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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