A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601151



Internal ID16388560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24323630..24327273hg38UCSC Ensembl
Innerchr6:24323858..24327501hg19UCSC Ensembl
Innerchr6:24431837..24435480hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg383644
hg193644
hg183644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10328n54
Supporting Variantsnssv1051251
Samples
Known GenesDCDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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