A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596160



Internal ID21544767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71468973..71469236hg38UCSC Ensembl
chr14:71935690..71935953hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085216
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596160
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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