A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596083



Internal ID21544690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75599184..75623900hg38UCSC Ensembl
chr16:75633082..75657798hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3824717
hg1924717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096072
SamplesHG02492
Known GenesADAT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596083
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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