A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060471



Internal ID19149690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58351479..58383250hg38UCSC Ensembl
Innerchr16:58385383..58417154hg19UCSC Ensembl
Innerchr16:56942884..56974655hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3831772
hg1931772
hg1831772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2990n100
Supporting Variantsnssv3559356
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)nsv1060471
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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