A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750696



Internal ID20526617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37562949..37562949hg38UCSC Ensembl
chr3:37604440..37604440hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266922
Samples
Known GenesITGA9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750696
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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