A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288606



Internal ID20497824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74994721..74995040hg38UCSC Ensembl
chr14:75461424..75461743hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288606
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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