A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568261



Internal ID16355670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22788625..22997016hg38UCSC Ensembl
Innerchr15:22876052..23084443hg19UCSC Ensembl
Innerchr15:20427493..20635884hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38208392
hg19208392
hg18208392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4322n54
Supporting Variantsnssv1148657
Samples1780862356_A
Known GenesCYFIP1, NIPA1, NIPA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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