A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604130



Internal ID16391539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90296236..90299188hg38UCSC Ensembl
Innerchr6:91005955..91008907hg19UCSC Ensembl
Innerchr6:91062676..91065628hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382953
hg192953
hg182953
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1068397
Samples
Known GenesBACH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604130
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