A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv886538



Internal ID6293549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111111127..111399790hg19UCSC Ensembl
Outerchr6:111073363..111415640hg19UCSC Ensembl
Innerchr6:111217820..111506483hg18UCSC Ensembl
Outerchr6:111180056..111522333hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1534859
SamplesMS11746
Known GenesAMD1, CDK19, GSTM2P1, GTF3C6, RPF2, SLC16A10
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv886538
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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