A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv882903



Internal ID6289914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131665378..131732456hg19UCSC Ensembl
Outerchr5:131663062..131743777hg19UCSC Ensembl
Innerchr5:131693277..131760355hg18UCSC Ensembl
Outerchr5:131690961..131771676hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1541790
SamplesMS15491
Known GenesLOC553103, MIR3936, SLC22A4, SLC22A5
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv882903
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