A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708840



Internal ID15656110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3195184..3221547hg38UCSC Ensembl
Innerchr1:3111748..3138111hg19UCSC Ensembl
Innerchr1:3101608..3127971hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3826364
hg1926364
hg1826364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545120
Supporting Variants
Samples
Known GenesPRDM16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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