A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042048



Internal ID19131267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47463335..47542736hg38UCSC Ensembl
Innerchr15:47755532..47834933hg19UCSC Ensembl
Innerchr15:45542824..45622225hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3879402
hg1979402
hg1879402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552376
Samples
Known GenesSEMA6D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042048
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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