A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598011



Internal ID21546632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127961761..127961852hg38UCSC Ensembl
chr9:130724040..130724131hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159924
SamplesHG00513
Known GenesFAM102A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598011
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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