A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569342



Internal ID16010065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49237105..49257746hg38UCSC Ensembl
Innerchr15:49529302..49549943hg19UCSC Ensembl
Innerchr15:47316594..47337235hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3820642
hg1920642
hg1820642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842501
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569342
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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