A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569333



Internal ID16356742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:47301537..47359165hg38UCSC Ensembl
Innerchr15:47593734..47651362hg19UCSC Ensembl
Innerchr15:45381026..45438654hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3857629
hg1957629
hg1857629
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149595
Samples1782681096_A
Known GenesSEMA6D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569333
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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