A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568865



Internal ID16009588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32159287..32565013hg38UCSC Ensembl
Innerchr15:32451488..32857214hg19UCSC Ensembl
Innerchr15:30238780..30644506hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38405727
hg19405727
hg18405727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4446n54
Supporting Variantsnssv839714
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568865
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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