A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039827



Internal ID18782358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34464686..34538731hg38UCSC Ensembl
Innerchr15:34756887..34830932hg19UCSC Ensembl
Innerchr15:32544179..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3874046
hg1974046
hg1874046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2572n100
Supporting Variantsnssv3552129, nssv3716655
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039827
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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