A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161068



Internal ID21475617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135518594..135518644hg38UCSC Ensembl
chr9:138410440..138410490hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586333
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161068
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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