A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162442



Internal ID21493391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69843551..69843601hg38UCSC Ensembl
chr9:72458467..72458517hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589888
Supporting Variants
SamplesNA19238
Known GenesC9orf135
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162442
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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