A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569992



Internal ID16357401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74839978..74845527hg38UCSC Ensembl
Innerchr15:75132319..75137868hg19UCSC Ensembl
Innerchr15:72919372..72924921hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg385550
hg195550
hg185550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845286
Samples
Known GenesMIR6882, SCAMP2, ULK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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