A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050893



Internal ID18793424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:111939..155667hg38UCSC Ensembl
Innerchr16:161938..205666hg19UCSC Ensembl
Innerchr16:101938..145666hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3843729
hg1943729
hg1843729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556943
Samples
Known GenesHBZ, NPRL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050893
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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