A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600847



Internal ID16041570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3254222..3254929hg38UCSC Ensembl
Innerchr6:3254456..3255163hg19UCSC Ensembl
Innerchr6:3199455..3200162hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38708
hg19708
hg18708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10275n54
Supporting Variantsnssv1048688
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600847
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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