A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594592



Internal ID21543191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58119773..58119848hg38UCSC Ensembl
chr16:58153677..58153752hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081271
SamplesHG00512
Known GenesC16orf80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594592
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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