A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978073



Internal ID18266592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32478861..32592626hg38UCSC Ensembl
Innerchr16:32490182..32603947hg19UCSC Ensembl
Innerchr16:32397683..32511448hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38113766
hg19113766
hg18113766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34n82
Supporting Variantsnssv2641169, nssv2641165, nssv2641162, nssv2641166, nssv2641161, nssv2641167, nssv2641164, nssv2641160, nssv2641163, nssv2641168
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978073
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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