A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433323



Internal ID21395325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9957984..9962421hg38UCSC Ensembl
chr20:9938632..9943069hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg384438
hg194438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747469
SamplesNB08
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433323
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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