A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603011



Internal ID16043734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:46338611..46339765hg38UCSC Ensembl
Innerchr6:46306348..46307502hg19UCSC Ensembl
Innerchr6:46414307..46415461hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg381155
hg191155
hg181155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1058428
Samples
Known GenesRCAN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603011
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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