A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265057



Internal ID20474275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121641976..121642032hg38UCSC Ensembl
chr9:124404255..124404311hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742284
Supporting Variants
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265057
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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