A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7948n223



Internal ID22810916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129428101..129444000hg38UCSC Ensembl
chr9:132190380..132206279hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3815900
hg1915900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6452264, nsv6439553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7948n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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