A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831803



Internal ID6157527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:167184717..167365777hg19UCSC Ensembl
Outerchr1:165451341..165632401hg18UCSC Ensembl
Outerchr1:163916375..164097435hg17UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1451139
Samples
Known GenesPOU2F1
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831803
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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