A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983008



Internal ID18618202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45513408..45515232hg38UCSC Ensembl
Innerchr11:45534958..45536782hg19UCSC Ensembl
Innerchr11:45491534..45493358hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381825
hg191825
hg181825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1883879, nssv1883876, nssv1883878, nssv1883883, nssv1883877, nssv1883880, nssv1883881, nssv1883882, nssv1883875, nssv1883874
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)nsv983008
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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