A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599937



Internal ID21548575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65060426..65060709hg38UCSC Ensembl
chr14:65527144..65527427hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085616
SamplesHG00731
Known GenesCHURC1-FNTB, FNTB, MAX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599937
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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