A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545122



Internal ID15985845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3299553..3300455hg38UCSC Ensembl
Innerchr1:3216117..3217019hg19UCSC Ensembl
Innerchr1:3205977..3206879hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38903
hg19903
hg18903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv708842
Samples
Known GenesPRDM16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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