A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589518



Internal ID21538082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:138234775..138234828hg38UCSC Ensembl
chr9:141125225..141125278hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161005
SamplesHG03125
Known GenesFAM157B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589518
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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