A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977902



Internal ID18266421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10929005..10929505hg38UCSC Ensembl
Innerchr16:11022862..11023362hg19UCSC Ensembl
Innerchr16:10930363..10930863hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2042766, nssv2042758, nssv2042757, nssv2042760, nssv2042762, nssv2042763, nssv2042764, nssv2042759, nssv2042761, nssv2042765
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesDEXI
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977902
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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