A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590599



Internal ID16031322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71582455..71585992hg38UCSC Ensembl
Innerchr3:71631606..71635143hg19UCSC Ensembl
Innerchr3:71714296..71717833hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383538
hg193538
hg183538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965541, nssv965540
Samples
Known GenesFOXP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590599
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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