A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045181



Internal ID19134400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13316964..13346851hg38UCSC Ensembl
Innerchr16:13410821..13440708hg19UCSC Ensembl
Innerchr16:13318322..13348209hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3829888
hg1929888
hg1829888
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2737n100
Supporting Variantsnssv3557227
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)nsv1045181
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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