A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591005



Internal ID21539577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128356700..128356849hg38UCSC Ensembl
chr9:131118979..131119128hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160291
SamplesHG00513
Known GenesSLC27A4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591005
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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