A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047719



Internal ID18790250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34376855..34585552hg38UCSC Ensembl
Innerchr15:34669056..34877753hg19UCSC Ensembl
Innerchr15:32456348..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38208698
hg19208698
hg18208698
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2550n100
Supporting Variantsnssv3547876
Samples
Known GenesGOLGA8A, GOLGA8B, 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)nsv1047719
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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