A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17149086



Internal ID21422919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104638692..104639005hg38UCSC Ensembl
chr9:107400973..107401286hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604090
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17149086
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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