A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568816



Internal ID16356225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483399..31484247hg38UCSC Ensembl
Innerchr15:31775602..31776450hg19UCSC Ensembl
Innerchr15:29562894..29563742hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38849
hg19849
hg18849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4438n54
Supporting Variantsnssv839629
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568816
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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