A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041830



Internal ID18784361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34488426..34565797hg38UCSC Ensembl
Innerchr15:34780627..34857998hg19UCSC Ensembl
Innerchr15:32567919..32645290hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3877372
hg1977372
hg1877372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2574n100
Supporting Variantsnssv3716658, nssv3716657, nssv3716659
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)nsv1041830
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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