A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605262



Internal ID16392671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:166748083..166749430hg38UCSC Ensembl
Innerchr6:167161571..167162918hg19UCSC Ensembl
Innerchr6:167081561..167082908hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381348
hg191348
hg181348
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11041n54
Supporting Variantsnssv1076266, nssv1076265
Samples
Known GenesRPS6KA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605262
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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