A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552062



Internal ID15992785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:104254126..104282744hg38UCSC Ensembl
Innerchr10:106013884..106042502hg19UCSC Ensembl
Innerchr10:106003874..106032492hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3828619
hg1928619
hg1828619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv756080
Samples
Known GenesGSTO1, GSTO2, MIR4482-1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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