A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599481



Internal ID21548115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91293279..91293540hg38UCSC Ensembl
chr14:91759623..91759884hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086890
SamplesNA19239
Known GenesCCDC88C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599481
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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