A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601150



Internal ID16388559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24323630..24326368hg38UCSC Ensembl
Innerchr6:24323858..24326596hg19UCSC Ensembl
Innerchr6:24431837..24434575hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg382739
hg192739
hg182739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10328n54
Supporting Variantsnssv1051250, nssv1051249, nssv1051248
Samples
Known GenesDCDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601150
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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