A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568227



Internal ID16008950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22606432..23121326hg38UCSC Ensembl
Innerchr15:22751742..23266664hg19UCSC Ensembl
Innerchr15:20303106..20818105hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38514895
hg19514923
hg18515000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4318n54
Supporting Variantsnssv838340, nssv838339
Samples
Known GenesCYFIP1, GOLGA8I, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568227
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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