A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583804



Internal ID21532334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108930496..108930626hg38UCSC Ensembl
chr1:109473118..109473248hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17060283
SamplesHG03065
Known GenesCLCC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583804
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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