A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601214



Internal ID16041937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28968779..29369723hg38UCSC Ensembl
Innerchr6:28936556..29337500hg19UCSC Ensembl
Innerchr6:29044535..29445479hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38400945
hg19400945
hg18400945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10338n54
Supporting Variantsnssv1051659
Samples
Known GenesLOC100129636, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, OR5V1, ZNF311
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601214
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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