A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1053288



Internal ID15906474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31340853..31354782hg38UCSC Ensembl
Innerchr6:31308630..31322559hg19UCSC Ensembl
Innerchr6:31416609..31430538hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3813930
hg1913930
hg1813930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601821
Supporting Variants
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1053288
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