A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089089



Internal ID21486610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111545482..111545789hg38UCSC Ensembl
chr13:112197829..112198136hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591835
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089089
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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