A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050707



Internal ID18793238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34431219..34538040hg38UCSC Ensembl
Innerchr15:34723420..34830241hg19UCSC Ensembl
Innerchr15:32510712..32617533hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38106822
hg19106822
hg18106822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2557n100
Supporting Variantsnssv3721932
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)nsv1050707
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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