A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594685



Internal ID21543285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84167742..84384775hg38UCSC Ensembl
chr16:84201348..84418381hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38217034
hg19217034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092323
SamplesHG03009
Known GenesADAD2, ATP2C2, DNAAF1, KCNG4, TAF1C, WFDC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594685
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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