A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392534



Internal ID21383564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32723064..32724971hg38UCSC Ensembl
chr20:31310871..31312778hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381908
hg191908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706530
Samples
Known GenesCOMMD7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392534
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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