A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975897



Internal ID18611104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29275448..29276737hg38UCSC Ensembl
Innerchr11:29296995..29298284hg19UCSC Ensembl
Innerchr11:29253571..29254860hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381290
hg191290
hg181290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879829, nssv1879824, nssv1879826, nssv1879825, nssv1879830, nssv1879828, nssv1879823, nssv1879832, nssv1879827, nssv1879831
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)nsv975897
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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