A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469714



Internal ID22527604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86938299..86940898hg38UCSC Ensembl
chr14:87404643..87407242hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469714
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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