A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458229



Internal ID22516110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25184107..25186445hg38UCSC Ensembl
chr14:25653313..25655651hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382339
hg192339
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458229
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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