A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195396



Internal ID20762436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35148241..35222452hg38UCSC Ensembl
chr14:35617447..35691658hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3874212
hg1974212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484115
Supporting Variants
Samples
Known GenesKIAA0391
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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