A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603583



Internal ID16390992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:66852051..66914446hg38UCSC Ensembl
Innerchr6:67561944..67624339hg19UCSC Ensembl
Innerchr6:67618665..67681060hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3862396
hg1962396
hg1862396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10749n54
Supporting Variantsnssv1063561
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603583
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