A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045753



Internal ID19134972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32269465..32550909hg38UCSC Ensembl
Innerchr15:32561666..32843110hg19UCSC Ensembl
Innerchr15:30348958..30630402hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38281445
hg19281445
hg18281445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3547860
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)nsv1045753
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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