A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037878



Internal ID19127097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92169900..92196597hg38UCSC Ensembl
Innerchr15:92713130..92739827hg19UCSC Ensembl
Innerchr15:90514134..90540831hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3826698
hg1926698
hg1826698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555225
Samples
Known GenesSLCO3A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037878
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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