A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586568



Internal ID21535122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36270290..36271869hg38UCSC Ensembl
chr21:37642588..37644167hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg381580
hg191580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118565
SamplesHG03486
Known GenesDOPEY2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586568
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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