A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049514



Internal ID18792045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41666284..41789012hg38UCSC Ensembl
Innerchr15:41958482..42081210hg19UCSC Ensembl
Innerchr15:39745774..39868502hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38122729
hg19122729
hg18122729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552259
Samples
Known GenesMAPKBP1, MGA, MIR626
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049514
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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