A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586401



Internal ID21534954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44764167..44764252hg38UCSC Ensembl
chr21:46184082..46184167hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118750
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586401
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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