A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046481



Internal ID19135700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19928432..19959156hg38UCSC Ensembl
Innerchr16:19939754..19970478hg19UCSC Ensembl
Innerchr16:19847255..19877979hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3830725
hg1930725
hg1830725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2790n100
Supporting Variantsnssv3542775
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)nsv1046481
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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