A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055662



Internal ID15908848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32536048..32584162hg38UCSC Ensembl
Innerchr6:32503825..32551939hg19UCSC Ensembl
Innerchr6:32611803..32659917hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3848115
hg1948115
hg1848115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602467
Supporting Variants
Samples
Known GenesHLA-DRB1, HLA-DRB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1055662
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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