A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589097



Internal ID21537661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13675079..13675529hg38UCSC Ensembl
chr18:13675078..13675528hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100513
SamplesNA19238
Known GenesFAM210A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589097
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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