A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159868



Internal ID21493764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121649215..121649516hg38UCSC Ensembl
chr9:124411494..124411795hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600183
Supporting Variants
SamplesNA19238
Known GenesDAB2IP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159868
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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