A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586152



Internal ID21534702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92850945..92852611hg38UCSC Ensembl
chr14:93317290..93318956hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381667
hg191667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086721
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586152
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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