A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602508



Internal ID16389917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32552256..32554371hg38UCSC Ensembl
Innerchr6:32520033..32522148hg19UCSC Ensembl
Innerchr6:32628011..32630126hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382116
hg192116
hg182116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1055716
Samples
Known GenesHLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602508
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