A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450280



Internal ID22508150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28402438..28409145hg38UCSC Ensembl
chr14:28871644..28878351hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg386708
hg196708
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864971
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450280
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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