A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638922



Internal ID21587227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112138238..112138238hg38UCSC Ensembl
chr9:114900518..114900518hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159634
SamplesHG00731
Known GenesMIR3134, SUSD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638922
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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