A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975950



Internal ID18611157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77312929..77316286hg38UCSC Ensembl
Innerchr11:77023974..77027331hg19UCSC Ensembl
Innerchr11:76701622..76704979hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg383358
hg193358
hg183358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1896631, nssv1896628, nssv1896633, nssv1896632, nssv1896625, nssv1896630, nssv1896626, nssv1896634, nssv1896627, nssv1896629
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)nsv975950
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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