A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935715



Internal ID22711060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10233258..10233395hg38UCSC Ensembl
chr20:10213906..10214043hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399982
Samples
Known GenesSNAP25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935715
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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