A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590143



Internal ID21538712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16397926..16398052hg38UCSC Ensembl
chr21:17770246..17770372hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119244
SamplesHG03486
Known GenesLINC00478
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590143
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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