A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601826



Internal ID16389235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31344034..31372067hg38UCSC Ensembl
Innerchr6:31311811..31339844hg19UCSC Ensembl
Innerchr6:31419790..31447823hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3828034
hg1928034
hg1828034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10440n54
Supporting Variantsnssv1053302
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601826
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