A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390923



Internal ID21048476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152490768..152491499hg38UCSC Ensembl
chr4:153411920..153412651hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112026
Samples
Known GenesFBXW7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390923
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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