A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585011



Internal ID21533555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92929294..92929373hg38UCSC Ensembl
chr14:93395639..93395718hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082635
SamplesHG00731
Known GenesCHGA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585011
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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