A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039020



Internal ID18781551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34447659..34538175hg38UCSC Ensembl
Innerchr15:34739860..34830376hg19UCSC Ensembl
Innerchr15:32527152..32617668hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3890517
hg1990517
hg1890517
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2562n100
Supporting Variantsnssv3551706, nssv3551707, nssv3551705
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)nsv1039020
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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