A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051244



Internal ID15904430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24166005..24215437hg38UCSC Ensembl
Innerchr6:24166233..24215665hg19UCSC Ensembl
Innerchr6:24274212..24323644hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3849433
hg1949433
hg1849433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601146
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)nssv1051244
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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