A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975877



Internal ID18264398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6485212..6488986hg38UCSC Ensembl
Innerchr11:6506442..6510216hg19UCSC Ensembl
Innerchr11:6463018..6466792hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383775
hg193775
hg183775
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1875815, nssv1875824, nssv1875823, nssv1875816, nssv1875818, nssv1875819, nssv1875821, nssv1875820, nssv1875817, nssv1875822
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)nsv975877
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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