A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041460



Internal ID19130679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60935507..61002693hg38UCSC Ensembl
Innerchr15:61227706..61294892hg19UCSC Ensembl
Innerchr15:59014998..59082184hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3867187
hg1967187
hg1867187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553625
Samples
Known GenesRORA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041460
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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