A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10479n54



Internal ID20143903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32011830..32023513hg38UCSC Ensembl
chr6:31979607..31991290hg19UCSC Ensembl
chr6:32087585..32099268hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3811684
hg1911684
hg1811684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv602070, nsv602069, nsv602068
Samples
Known GenesC4A, C4B, C4B_2, STK19, TNXA, TNXB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10479n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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