A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979677



Internal ID18614878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39318355..39318855hg38UCSC Ensembl
Innerchr22:39714360..39714860hg19UCSC Ensembl
Innerchr22:38044306..38044806hg18UCSC Ensembl
Cytoband22q13.1
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 Variantsnssv2266836, nssv2266841, nssv2266839, nssv2266840, nssv2266844, nssv2266835, nssv2266837, nssv2266843, nssv2266842, nssv2266838
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesRPL3
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv979677
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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