A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188066



Internal ID20755106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:106219756..106768456hg38UCSC Ensembl
chr14:106676400..107176698hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38548701
hg19500299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499078
Supporting Variants
Samples
Known GenesLINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188066
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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