A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054807



Internal ID19144026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9239837..9298524hg38UCSC Ensembl
Innerchr16:9333694..9392381hg19UCSC Ensembl
Innerchr16:9241195..9299882hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3858688
hg1958688
hg1858688
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557121
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)nsv1054807
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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