A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047892



Internal ID18790423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34447659..34538731hg38UCSC Ensembl
Innerchr15:34739860..34830932hg19UCSC Ensembl
Innerchr15:32527152..32618224hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3891073
hg1991073
hg1891073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2569n100
Supporting Variantsnssv3551719, nssv3551713, nssv3551722, nssv3551714, nssv3551710, nssv3552096, nssv3551712, nssv3552093, nssv3551716, nssv3551721, nssv3551708, nssv3551718, nssv3551709, nssv3552095, nssv3716654, nssv3552094, nssv3551720, nssv3551715, nssv3551711, nssv3551717, nssv3551723
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)nsv1047892
Frequency
Sample Size29084
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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