A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763832



Internal ID20539692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125577542..125577542hg38UCSC Ensembl
chr9:128339821..128339821hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271449
Samples
Known GenesMAPKAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763832
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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