A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194752



Internal ID20761792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:43876792..44392027hg38UCSC Ensembl
chr14:44345995..44861230hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38515236
hg19515236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194752
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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