A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601672



Internal ID16389081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31314361..31347388hg38UCSC Ensembl
Innerchr6:31282138..31315165hg19UCSC Ensembl
Innerchr6:31390117..31423144hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3833028
hg1933028
hg1833028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053034
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601672
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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