A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588501



Internal ID21537064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10764742..10764847hg38UCSC Ensembl
chr16:10858599..10858704hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080868
SamplesHG00731
Known GenesNUBP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588501
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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