A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588803



Internal ID21537367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77828826..77830732hg38UCSC Ensembl
chr14:78295169..78297075hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381907
hg191907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080843
SamplesHG00732
Known GenesADCK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588803
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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