A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599134



Internal ID21547767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11880054..11880365hg38UCSC Ensembl
chr18:11880053..11880364hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100584
SamplesNA20847
Known GenesGNAL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599134
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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