A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023567



Internal ID19112784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32481273..32550980hg38UCSC Ensembl
Innerchr6:32449050..32518757hg19UCSC Ensembl
Innerchr6:32557028..32626735hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3869708
hg1969708
hg1869708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5946n100
Supporting Variantsnssv3655965, nssv3655964, nssv3655963, nssv3655966, nssv3655967, nssv3655962
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023567
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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