A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956101



Internal ID22731293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62992192..62993888hg38UCSC Ensembl
chr20:61623544..61625240hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381697
hg191697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956101
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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