A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161007



Internal ID21499203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13840779..13841082hg38UCSC Ensembl
chr9:13840778..13841081hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596789
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161007
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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