A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596259



Internal ID21544866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69946552..70169466hg38UCSC Ensembl
chr16:69980455..70203369hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38222915
hg19222915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089522
SamplesNA19238
Known GenesCLEC18A, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596259
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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