A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950269



Internal ID22725675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33713947..33714002hg38UCSC Ensembl
chr20:32301753..32301808hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399040
Samples
Known GenesPXMP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950269
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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