A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039529



Internal ID18782060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430431..34538040hg38UCSC Ensembl
Innerchr15:34722632..34830241hg19UCSC Ensembl
Innerchr15:32509924..32617533hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38107610
hg19107610
hg18107610
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2562n100
Supporting Variantsnssv3549519, nssv3721873
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)nsv1039529
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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