A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432261



Internal ID21394263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77616659..77619658hg38UCSC Ensembl
chr15:77909001..77912000hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv264n172
Supporting Variantsnssv15749547, nssv15747277, nssv15751872, nssv15750841, nssv15748085, nssv15747343, nssv15750000, nssv15752900, nssv15752895
SamplesNB12, MDQ045, BTQ038, BTQ055, BTQ016, NB11, NB07, SMI018, NB09
Known GenesLINGO1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432261
Frequency
Sample Size15
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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