A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628869



Internal ID21577174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74318234..74318234hg38UCSC Ensembl
chr9:76933150..76933150hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162803
SamplesHG03009
Known GenesMIR6130
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628869
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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