A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749887



Internal ID21385264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76977400..76979392hg38UCSC Ensembl
chr14:77443743..77445735hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381993
hg191993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432143
Supporting Variants
SamplesBTQ055
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749887
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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