A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049632



Internal ID19138851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13316964..13345027hg38UCSC Ensembl
Innerchr16:13410821..13438884hg19UCSC Ensembl
Innerchr16:13318322..13346385hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3828064
hg1928064
hg1828064
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2737n100
Supporting Variantsnssv3557226
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)nsv1049632
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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