A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192883



Internal ID20759923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34109501..34153700hg38UCSC Ensembl
chr14:34578707..34622906hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3844200
hg1944200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192883
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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