A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv872534



Internal ID6279545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169535918..169560485hg19UCSC Ensembl
Outerchr1:169533266..169561274hg19UCSC Ensembl
Innerchr1:167802542..167827109hg18UCSC Ensembl
Outerchr1:167799890..167827898hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1514499
SamplesSP56007
Known GenesF5, SELP
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv872534
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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