A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569233



Internal ID16009956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41492611..41513039hg38UCSC Ensembl
Innerchr15:41784809..41805237hg19UCSC Ensembl
Innerchr15:39572101..39592529hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3820429
hg1920429
hg1820429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842224
Samples
Known GenesITPKA, LTK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569233
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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