A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037543



Internal ID19126762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32283629..32623392hg38UCSC Ensembl
Innerchr15:32575830..32915593hg19UCSC Ensembl
Innerchr15:30363122..30702885hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38339764
hg19339764
hg18339764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3721657
Samples
Known GenesARHGAP11A, GOLGA8K, GOLGA8O, GOLGA8R, 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)nsv1037543
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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