A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043349



Internal ID18785880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34488426..34570510hg38UCSC Ensembl
Innerchr15:34780627..34862711hg19UCSC Ensembl
Innerchr15:32567919..32650003hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3882085
hg1982085
hg1882085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2574n100
Supporting Variantsnssv3716660
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)nsv1043349
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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