A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055833



Internal ID19145052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:47742927..47841698hg38UCSC Ensembl
Innerchr16:47776838..47875609hg19UCSC Ensembl
Innerchr16:46334339..46433110hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3898772
hg1998772
hg1898772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722704
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)nsv1055833
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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