A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660103



Internal ID21608408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24023974..24023974hg38UCSC Ensembl
chr18:21603938..21603938hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101078
SamplesHG03486
Known GenesTTC39C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660103
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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