A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055106



Internal ID19144325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32283629..32565269hg38UCSC Ensembl
Innerchr15:32575830..32857470hg19UCSC Ensembl
Innerchr15:30363122..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38281641
hg19281641
hg18281641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3547867
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)nsv1055106
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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