A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159776



Internal ID21452851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127509761..127509830hg38UCSC Ensembl
chr9:130272040..130272109hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588569
Supporting Variants
SamplesHG02011
Known GenesFAM129B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159776
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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