A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588895



Internal ID21537459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43669088..43669144hg38UCSC Ensembl
chr21:45088969..45089025hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118682
SamplesHG03486
Known GenesRRP1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588895
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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