A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951569



Internal ID22726929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20272947..20274820hg38UCSC Ensembl
chr20:20253591..20255464hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg381874
hg191874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403447
Samples
Known GenesC20orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951569
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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