A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603134



Internal ID16390543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54976874..54986542hg38UCSC Ensembl
Innerchr6:54841672..54851340hg19UCSC Ensembl
Innerchr6:54949631..54959299hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg389669
hg199669
hg189669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1060758
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603134
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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