A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040206



Internal ID18782737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32497505hg38UCSC Ensembl
Innerchr15:32539525..32789706hg19UCSC Ensembl
Innerchr15:30326817..30576998hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38250182
hg19250182
hg18250182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2546n100
Supporting Variantsnssv3547810
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)nsv1040206
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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