A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761102



Internal ID20536962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100309758..100309758hg38UCSC Ensembl
chr9:103072040..103072040hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259460
Samples
Known GenesTEX10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761102
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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