A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601935



Internal ID16042658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31469528..31489801hg38UCSC Ensembl
Innerchr6:31437305..31457578hg19UCSC Ensembl
Innerchr6:31545284..31565557hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3820274
hg1920274
hg1820274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053517
Samples
Known GenesHCG26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601935
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