A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv264n172



Internal ID22814638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77615659..77619658hg38UCSC Ensembl
chr15:77908001..77912000hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4432261, nsv4432259
SamplesNB12, MDQ045, BTQ038, BTQ055, BTQ016, NB11, NB07, SMI018, MDQ025, NB09
Known GenesLINGO1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)dgv264n172
Frequency
Sample Size15
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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