A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv260n172



Internal ID22814634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62413774..62415707hg38UCSC Ensembl
chr15:62705973..62707906hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381934
hg191934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432243, nsv4432242, nsv4432241, nsv4432244
SamplesNB12, SMI034, MDQ045, BTQ038, NB10, BTQ055, MDQ010, BTQ016, SMI041, NB11, SMI018, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv260n172
Frequency
Sample Size15
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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