A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17470329



Internal ID22528219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86145117..86148386hg38UCSC Ensembl
chr14:86611461..86614730hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg383270
hg193270
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17470329
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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