A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061754



Internal ID19150973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33573405..34124742hg38UCSC Ensembl
Innerchr16:33375872..33927209hg19UCSC Ensembl
Innerchr16:33283373..33834710hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38551338
hg19551338
hg18551338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2915n100
Supporting Variantsnssv3553476
Samples
Known GenesRNU6-76P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061754
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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