A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051799



Internal ID15558299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29952688hg38UCSC Ensembl
Innerchr6:29851443..29920465hg19UCSC Ensembl
Innerchr6:29959422..30028444hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3869023
hg1969023
hg1869023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601263
Supporting Variants
Samples
Known GenesHCG4B, HLA-A, HLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051799
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