A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455186



Internal ID22513063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100213674..100221957hg38UCSC Ensembl
chr14:100680011..100688294hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg388284
hg198284
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857374
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455186
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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