A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958166



Internal ID22733242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43568422..43568716hg38UCSC Ensembl
chr20:42197062..42197356hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404786
Samples
Known GenesSGK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958166
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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