A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956226



Internal ID22731418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53499628..53535915hg38UCSC Ensembl
chr20:52116167..52152454hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3836288
hg1936288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956226
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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