A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568341



Internal ID16355750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23452861..23678428hg38UCSC Ensembl
Innerchr15:23698008..23923575hg19UCSC Ensembl
Innerchr15:21249101..21474668hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38225568
hg19225568
hg18225568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv838506
Samples
Known GenesMAGEL2, MIR4508, MKRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568341
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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