A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596803



Internal ID21545412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57486753..57486821hg38UCSC Ensembl
chr16:57520665..57520733hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089938
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596803
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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