A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610206



Internal ID16050929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:9103507..9304538hg38UCSC Ensembl
Innerchr8:8961017..9162048hg19UCSC Ensembl
Innerchr8:8998427..9199458hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38201032
hg19201032
hg18201032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1105989
Samples
Known GenesPPP1R3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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