A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978210



Internal ID18266729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28756059..28757460hg38UCSC Ensembl
Innerchr16:28767380..28768781hg19UCSC Ensembl
Innerchr16:28674881..28676282hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381402
hg191402
hg181402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2635884, nssv2635886, nssv2635878, nssv2635882, nssv2635881, nssv2635887, nssv2635885, nssv2635880, nssv2635879, nssv2635883
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978210
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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