A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470355



Internal ID22528245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92872489..92873564hg38UCSC Ensembl
chr14:93338834..93339909hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470355
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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