A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112966



Internal ID21296232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8048744..8053014hg38UCSC Ensembl
Innerchr10:8090707..8094977hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg384271
hg194271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089858
Samplessample373
Known GenesGATA3-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112966
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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