A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196929



Internal ID20763969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93947922..94028320hg38UCSC Ensembl
chr14:94414268..94494666hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3880399
hg1980399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514661
Supporting Variants
Samples
Known GenesASB2, LINC00521, OTUB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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