A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604451



Internal ID21553120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25677894..25678250hg38UCSC Ensembl
chr14:26147100..26147456hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082323
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604451
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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