A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600738



Internal ID16388147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:175522..249597hg38UCSC Ensembl
Innerchr6:175522..249597hg19UCSC Ensembl
Innerchr6:120522..194597hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3874076
hg1974076
hg1874076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10256n54
Supporting Variantsnssv1047555
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600738
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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