A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1054842



Internal ID15908028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32491135..32581498hg38UCSC Ensembl
Innerchr6:32458912..32549275hg19UCSC Ensembl
Innerchr6:32566890..32657253hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3890364
hg1990364
hg1890364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602261
Supporting Variants
Samples
Known GenesHLA-DRB1, HLA-DRB5, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1054842
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