A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452552



Internal ID22510425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21581795..21590631hg38UCSC Ensembl
chr14:22049930..22058750hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg388837
hg198821
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452552
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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