A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742284



Internal ID20518266
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 StatusM
Merged Variants
Supporting Variantsnssv16265057
Samples
Known GenesDAB2IP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742284
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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