A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391243



Internal ID21382273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69523194..69524522hg38UCSC Ensembl
chr4:70388912..70390240hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381329
hg191329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703107
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391243
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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