A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047437



Internal ID19136656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32257489..32565269hg38UCSC Ensembl
Innerchr15:32549690..32857470hg19UCSC Ensembl
Innerchr15:30336982..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38307781
hg19307781
hg18307781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3547851, nssv3547849, nssv3547853, nssv3547850, nssv3547852
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)nsv1047437
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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