A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059033



Internal ID19148252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:24448409..24491411hg38UCSC Ensembl
Innerchr16:24459730..24502732hg19UCSC Ensembl
Innerchr16:24367231..24410233hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3843003
hg1943003
hg1843003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549127
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)nsv1059033
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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