A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568260



Internal ID16355669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22788625..23002268hg38UCSC Ensembl
Innerchr15:22870800..23084443hg19UCSC Ensembl
Innerchr15:20422241..20635884hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38213644
hg19213644
hg18213644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4322n54
Supporting Variantsnssv838386
Samples
Known GenesCYFIP1, NIPA1, NIPA2, TUBGCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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