A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1058199



Internal ID15564699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35411001..35489619hg38UCSC Ensembl
Innerchr6:35378778..35457396hg19UCSC Ensembl
Innerchr6:35486756..35565374hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3878619
hg1978619
hg1878619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602910
Supporting Variants
Samples
Known GenesFANCE, MIR7111, PPARD, RPL10A, TEAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1058199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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