A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182363



Internal ID20749403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103065408..103252792hg38UCSC Ensembl
chr14:103531745..103719129hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38187385
hg19187385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513714
Supporting Variants
Samples
Known GenesEXOC3L4, LINC00605, TNFAIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182363
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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