A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845259



Internal ID22620194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35600763..35606100hg38UCSC Ensembl
chr6:35568540..35573877hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385338
hg195338
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505347
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845259
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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