A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065358



Internal ID19154577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48479913..48520343hg38UCSC Ensembl
Innerchr16:48513824..48554254hg19UCSC Ensembl
Innerchr16:47071325..47111755hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3840431
hg1940431
hg1840431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559245
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)nsv1065358
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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