A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505289



Internal ID20878557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95320061..95667130hg38UCSC Ensembl
chr14:95786398..96133467hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38347070
hg19347070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188929
Samples
Known GenesGLRX5, LINC00341, SCARNA13, SNHG10, SYNE3, TCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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