A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469901



Internal ID6059674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132360176..132444099hg19UCSC Ensembl
Innerchr9:131399997..131483920hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv545915
SamplesHGDP00657
Known GenesASB6, C9orf50, METTL11A, PRRX2
Method
AnalysisOverlapping CNVs were merged. The positions are based on the farthest SNPs observed anomg any individuals with the CNV.
PlatformIllumina HumanHap550 Genotyping BeadChip v1 + v3
Comments
ReferenceJakobsson et al 2008
Pubmed ID18288195
Accession Number(s)nsv469901
Frequency
Sample Size443
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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