A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432543



Internal ID21394545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49059692..49060466hg38UCSC Ensembl
chr17:47137054..47137828hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752715
SamplesSMI018
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432543
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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