A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978008



Internal ID18266527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87977624..87994835hg38UCSC Ensembl
Innerchr16:88011230..88028441hg19UCSC Ensembl
Innerchr16:86568731..86585942hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3817212
hg1917212
hg1817212
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2069900, nssv2069901, nssv2069902, nssv2069897, nssv2069893, nssv2069896, nssv2069895, nssv2069894, nssv2069899, nssv2069898
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesBANP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978008
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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