A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947582



Internal ID22723089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40901771..40908107hg38UCSC Ensembl
chr20:39530411..39536747hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg386337
hg196337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947582
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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