A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604393



Internal ID16391802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104449043..104486604hg38UCSC Ensembl
Innerchr6:104896918..104934479hg19UCSC Ensembl
Innerchr6:105003611..105041172hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3837562
hg1937562
hg1837562
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10886n54
Supporting Variantsnssv1154858, nssv1071658
Samples1798860306_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604393
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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