A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950938



Internal ID22726327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20032015..20032456hg38UCSC Ensembl
chr20:20012659..20013100hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398473
Samples
Known GenesNAA20
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950938
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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