A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455383



Internal ID22513260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65266474..65275436hg38UCSC Ensembl
chr14:65733192..65742154hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg388963
hg198963
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862511
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455383
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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