A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392723



Internal ID21383753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152972828..152972912hg38UCSC Ensembl
chr6:153293963..153294047hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703973
Samples
Known GenesFBXO5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392723
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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