A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964494



Internal ID22739429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50907546..50907876hg38UCSC Ensembl
chr20:49524083..49524413hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17392897
Samples
Known GenesADNP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964494
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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