A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182892



Internal ID20749932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102092088..102097088hg38UCSC Ensembl
chr14:102558425..102563425hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501646
Supporting Variants
Samples
Known GenesHSP90AA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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