A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039166



Internal ID18781697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:104260183..104302423hg38UCSC Ensembl
Innerchr10:106019941..106062181hg19UCSC Ensembl
Innerchr10:106009931..106052171hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3842241
hg1942241
hg1842241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706213
Samples
Known GenesGSTO1, GSTO2, MIR4482-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039166
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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