A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587429



Internal ID21535989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35987427..35987578hg38UCSC Ensembl
chr18:33567390..33567541hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100881
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587429
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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