A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651173



Internal ID21599478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28156510..28156510hg38UCSC Ensembl
chr18:25736474..25736474hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100669
SamplesNA12878
Known GenesCDH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651173
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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