A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589286



Internal ID16030009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:227655..242064hg38UCSC Ensembl
Innerchr3:269338..283747hg19UCSC Ensembl
Innerchr3:244338..258747hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3814410
hg1914410
hg1814410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8151n54
Supporting Variantsnssv957799
Samples
Known GenesCHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589286
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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