A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615633



Internal ID21563938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:93265121..93265121hg38UCSC Ensembl
chr1:93730678..93730678hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067336
SamplesHG01114
Known GenesCCDC18
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615633
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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