A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv872n172



Internal ID22815246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134594155..134600154hg38UCSC Ensembl
chr9:137486001..137492000hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4435668, nsv4435670
SamplesMDQ045, MDQ010
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv872n172
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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