A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585650



Internal ID21534199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269715..77269800hg38UCSC Ensembl
chr14:77736058..77736143hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092122
SamplesHG00731
Known GenesNGB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585650
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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