A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222837



Internal ID20789877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35529096..35598377hg38UCSC Ensembl
chr6:35496873..35566154hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3869282
hg1969282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401440
Supporting Variants
Samples
Known GenesFKBP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00644


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