A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877542



Internal ID6284553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:138653488..138736641hg19UCSC Ensembl
Outerchr3:138645013..138750904hg19UCSC Ensembl
Innerchr3:140136178..140219331hg18UCSC Ensembl
Outerchr3:140127703..140233594hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546537
SamplesMS17208
Known GenesC3orf72, FOXL2, PRR23A, PRR23B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877542
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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