A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459152



Internal ID22517034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30069374..30072360hg38UCSC Ensembl
chr14:30538580..30541566hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382987
hg192987
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459152
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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