A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv864n172



Internal ID22815238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129424722..129444721hg38UCSC Ensembl
chr9:132187001..132207000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3820000
hg1920000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4435636, nsv4435638, nsv4435637
SamplesNB12, BTQ038, NB10, BTQ055, MDQ010, NB11, MDQ025, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv864n172
Frequency
Sample Size15
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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