A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145088



Internal ID21453147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109769069..109769121hg38UCSC Ensembl
chr9:112531349..112531401hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593051
Supporting Variants
SamplesHG02011
Known GenesPALM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145088
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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