A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602920



Internal ID16043643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35496996..35497817hg38UCSC Ensembl
Innerchr6:35464773..35465594hg19UCSC Ensembl
Innerchr6:35572751..35573572hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38822
hg19822
hg18822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10625n54
Supporting Variantsnssv1058208
Samples
Known GenesTEAD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602920
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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