A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587468



Internal ID21536028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101067255..101067305hg38UCSC Ensembl
chr13:101719607..101719657hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093562
SamplesHG00731
Known GenesNALCN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587468
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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