A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263329



Internal ID20472547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121734091..121734405hg38UCSC Ensembl
chr9:124496370..124496684hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735148
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263329
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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