A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505347



Internal ID22563291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35600763..35606100hg38UCSC Ensembl
chr6:35568540..35573877hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385338
hg195338
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845259
Supporting Variants
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505347
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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