A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159869



Internal ID21459742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121734082..121734397hg38UCSC Ensembl
chr9:124496361..124496676hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591516
Supporting Variants
SamplesHG02818
Known GenesDAB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159869
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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