A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058257



Internal ID19147476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52059637..52237903hg38UCSC Ensembl
Innerchr16:52093549..52271815hg19UCSC Ensembl
Innerchr16:50651050..50829316hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38178267
hg19178267
hg18178267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722707
Samples
Known GenesC16orf97, LINC00919, LOC102467079
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058257
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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