A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661783



Internal ID21610088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45411007..45411007hg38UCSC Ensembl
chr18:42990972..42990972hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101438
SamplesHG01596
Known GenesSLC14A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661783
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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