A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478665



Internal ID21136218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35127332..35257352hg38UCSC Ensembl
chr14:35596538..35726558hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38130021
hg19130021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017466
Samples
Known GenesKIAA0391
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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