A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048076



Internal ID19137295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32257489..32567645hg38UCSC Ensembl
Innerchr15:32549690..32859846hg19UCSC Ensembl
Innerchr15:30336982..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38310157
hg19310157
hg18310157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3547854, nssv3547856, nssv3547855
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048076
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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