A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959750



Internal ID22734772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53153272..53166231hg38UCSC Ensembl
chr20:51769811..51782770hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3812960
hg1912960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17408468
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959750
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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