A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190568



Internal ID20757608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95535227..96112095hg38UCSC Ensembl
chr14:96001564..96578432hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38576869
hg19576869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510019
Supporting Variants
Samples
Known GenesC14orf132, GLRX5, LINC00617, TCL1A, TCL1B, TCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190568
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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