A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041392



Internal ID18783923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87855368..87872753hg38UCSC Ensembl
Innerchr10:89615125..89632510hg19UCSC Ensembl
Innerchr10:89605105..89622490hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3817386
hg1917386
hg1817386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521722, nssv3514073
Samples
Known GenesKLLN, PTEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041392
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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