A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965331



Internal ID22740267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40586218..40586340hg38UCSC Ensembl
chr20:39214858..39214980hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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