A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388742



Internal ID21379877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9640314..9643446hg38UCSC Ensembl
chr8:9497824..9500956hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704339
Samples
Known GenesTNKS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388742
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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