A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068274



Internal ID21414663
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 StatusS
Merged Variantsnsv5571413
Supporting Variants
SamplesHG00513
Known GenesCLSTN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068274
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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