A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746319



Internal ID21387627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102761707..102762934hg38UCSC Ensembl
chr14:103228044..103229271hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432052
Supporting Variants
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746319
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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