A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391496



Internal ID21382526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9597434..9597568hg38UCSC Ensembl
chr16:9691291..9691425hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15705998
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391496
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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