A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568228



Internal ID16008951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22567965..23121326hg38UCSC Ensembl
Innerchr15:22751742..23305131hg19UCSC Ensembl
Innerchr15:20303106..20856572hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38553362
hg19553390
hg18553467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4318n54
Supporting Variantsnssv838341
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, 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)nsv568228
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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