A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392327



Internal ID21383357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35682054..35682134hg38UCSC Ensembl
chr6:35649831..35649911hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703755
Samples
Known GenesFKBP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392327
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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