A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604266



Internal ID21552933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:49820974..49821501hg38UCSC Ensembl
chr14:50287692..50288219hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090364
SamplesHG00731
Known GenesNEMF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604266
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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