A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391816



Internal ID21382846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52398542..52398998hg38UCSC Ensembl
chr17:50475902..50476358hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706175
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391816
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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