A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510019



Internal ID20883332
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 StatusM
Merged Variants
Supporting Variantsnssv18190568
Samples
Known GenesC14orf132, GLRX5, LINC00617, TCL1A, TCL1B, TCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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