A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975155



Internal ID18610363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17225805..17230558hg38UCSC Ensembl
Innerchr11:17247352..17252105hg19UCSC Ensembl
Innerchr11:17203928..17208681hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384754
hg194754
hg184754
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1876776, nssv1876779, nssv1876772, nssv1876774, nssv1876781, nssv1876778, nssv1876777, nssv1876773, nssv1876780, nssv1876775
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)nsv975155
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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