A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628763



Internal ID21577068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128808408..128808408hg38UCSC Ensembl
chr9:131570687..131570687hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160306
SamplesNA19650
Known GenesTBC1D13
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628763
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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