A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059847



Internal ID19149066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48948087..49041767hg38UCSC Ensembl
Innerchr16:48981998..49075678hg19UCSC Ensembl
Innerchr16:47539499..47633179hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3893681
hg1993681
hg1893681
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559250
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)nsv1059847
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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