A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096029



Internal ID21410827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110252468..110252533hg38UCSC Ensembl
chr13:110904815..110904880hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591733
Supporting Variants
SamplesHG00513
Known GenesCOL4A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096029
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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