A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160629



Internal ID21493644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13655412..13655743hg38UCSC Ensembl
chr9:13655411..13655742hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592416
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160629
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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