A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602248



Internal ID16389657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32520464hg38UCSC Ensembl
Innerchr6:32458912..32488241hg19UCSC Ensembl
Innerchr6:32566890..32596219hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3829330
hg1929330
hg1829330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10500n54
Supporting Variantsnssv1054727, nssv1054726
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602248
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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