A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014839



Internal ID21924182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35625836..35626068hg38UCSC Ensembl
chr6:35593613..35593845hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570366
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014839
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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