A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv872523



Internal ID6279534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:167184952..167370988hg19UCSC Ensembl
Outerchr1:167171571..167382374hg19UCSC Ensembl
Innerchr1:165451576..165637612hg18UCSC Ensembl
Outerchr1:165438195..165648998hg18UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1560666
SamplesMS24624
Known GenesPOU2F1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv872523
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer