A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049585



Internal ID18792116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32478247hg38UCSC Ensembl
Innerchr15:32539525..32770448hg19UCSC Ensembl
Innerchr15:30326817..30557740hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38230924
hg19230924
hg18230924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2546n100
Supporting Variantsnssv3547808, nssv3547809
Samples
Known GenesGOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049585
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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