A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038550



Internal ID18781081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435409..34585552hg38UCSC Ensembl
Innerchr15:34727610..34877753hg19UCSC Ensembl
Innerchr15:32514902..32665045hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38150144
hg19150144
hg18150144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3551611, nssv3551612
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)nsv1038550
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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