A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601185



Internal ID16041908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26455583..26465156hg38UCSC Ensembl
Innerchr6:26455811..26465384hg19UCSC Ensembl
Innerchr6:26563790..26573363hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg389574
hg199574
hg189574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051392
Samples
Known GenesBTN2A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601185
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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