A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601225



Internal ID16041948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29387371..29402508hg38UCSC Ensembl
Innerchr6:29355148..29370285hg19UCSC Ensembl
Innerchr6:29463127..29478264hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3815138
hg1915138
hg1815138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10340n54
Supporting Variantsnssv1051671
Samples
Known GenesOR12D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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