A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571413



Internal ID21519791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9786592..9796632hg38UCSC Ensembl
chr1:9846650..9856690hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3810041
hg1910041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068274
SamplesHG00513
Known GenesCLSTN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571413
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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