A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214537



Internal ID20781578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117368101..117379000hg38UCSC Ensembl
chr6:117689264..117700163hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606274
Supporting Variants
Samples
Known GenesROS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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