A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392733



Internal ID21383763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44173123..44173895hg38UCSC Ensembl
chr21:45593006..45593778hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706640
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392733
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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