A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051249



Internal ID15904435
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 StatusS
Merged Variantsnsv601150
Supporting Variants
Samples
Known GenesDCDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051249
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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