A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016092



Internal ID19105310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60688542..61082806hg38UCSC Ensembl
Innerchr6:57656289..58050553hg19UCSC Ensembl
Innerchr6:57764248..58158512hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38394265
hg19394265
hg18394265
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5971n100
Supporting Variantsnssv3657524
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016092
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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