A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928663



Internal ID22703906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23878543..23878607hg38UCSC Ensembl
chr14:24347752..24347816hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928663
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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