A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895403



Internal ID6302414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:54504049..54526762hg19UCSC Ensembl
Outerchr10:54501332..54529257hg19UCSC Ensembl
Innerchr10:54174055..54196768hg18UCSC Ensembl
Outerchr10:54171338..54199263hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1578756
SamplesIS34896
Known GenesMBL2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895403
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