A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190853



Internal ID20757893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100343120..100347820hg38UCSC Ensembl
chr14:100809457..100814157hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384701
hg194701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501032
Supporting Variants
Samples
Known GenesWARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190853
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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