A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880821



Internal ID22655791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20511293..20511775hg38UCSC Ensembl
chr1:20837786..20838268hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350821
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880821
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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