A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433316



Internal ID21395318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64117370..64119227hg38UCSC Ensembl
chr20:62748723..62750580hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753878
SamplesBTQ016
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433316
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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