A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568060



Internal ID16355469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22091136..22153760hg38UCSC Ensembl
Innerchr15:22379087..22441711hg19UCSC Ensembl
Innerchr15:19880451..19943075hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3862625
hg1962625
hg1862625
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4287n54
Supporting Variantsnssv838138
Samples
Known GenesOR4N3P, OR4N4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568060
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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