A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602558



Internal ID21551217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103883601..103883705hg38UCSC Ensembl
chr14:104349938..104350042hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085227
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602558
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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