A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940457



Internal ID22715866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10584227..10585855hg38UCSC Ensembl
chr20:10564875..10566503hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381629
hg191629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399547
Samples
Known GenesSLX4IP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940457
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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