A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020340



Internal ID19109559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32461817..32589524hg38UCSC Ensembl
Innerchr6:32429594..32557301hg19UCSC Ensembl
Innerchr6:32537572..32665279hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38127708
hg19127708
hg18127708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655910
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020340
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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