A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065125



Internal ID19154344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35237438..35468311hg38UCSC Ensembl
Innerchr16:34471809..34702682hg19UCSC Ensembl
Innerchr16:34329310..34560183hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38230874
hg19230874
hg18230874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558707
Samples
Known GenesLOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065125
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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