A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1055664



Internal ID15908850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32536098..32627446hg38UCSC Ensembl
Innerchr6:32503875..32595223hg19UCSC Ensembl
Innerchr6:32611853..32703201hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3891349
hg1991349
hg1891349
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602469
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)nssv1055664
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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