A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590598



Internal ID16031321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71582174..71583711hg38UCSC Ensembl
Innerchr3:71631325..71632862hg19UCSC Ensembl
Innerchr3:71714015..71715552hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381538
hg191538
hg181538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv965539
Samples
Known GenesFOXP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590598
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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