A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569212



Internal ID16356621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38973656..39328416hg38UCSC Ensembl
Innerchr15:39265857..39620617hg19UCSC Ensembl
Innerchr15:37053149..37407909hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38354761
hg19354761
hg18354761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv840711
Samples
Known GenesC15orf54
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569212
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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