A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581960



Internal ID21530466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:909450..909685hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150981
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581960
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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