A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17581102



Internal ID21773145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121734082..121734398hg38UCSC Ensembl
chr9:124496361..124496677hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015411
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17581102
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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