A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978176



Internal ID18613381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88110907..88138384hg38UCSC Ensembl
Innerchr16:88144513..88171990hg19UCSC Ensembl
Innerchr16:86702014..86729491hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3827478
hg1927478
hg1827478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2070055, nssv2070048, nssv2070051, nssv2070056, nssv2070052, nssv2070050, nssv2070054, nssv2070053, nssv2070049, nssv2070057
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv978176
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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