A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744151



Internal ID20520147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121092455..121092595hg38UCSC Ensembl
chr9:123854733..123854873hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266526
Samples
Known GenesCNTRL
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744151
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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