A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569426



Internal ID16356835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52721806..52754013hg38UCSC Ensembl
Innerchr15:53014003..53046210hg19UCSC Ensembl
Innerchr15:50801295..50833502hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3832208
hg1932208
hg1832208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843014
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569426
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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