A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975929



Internal ID18611136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56611681..56613519hg38UCSC Ensembl
Innerchr11:56379157..56380995hg19UCSC Ensembl
Innerchr11:56135733..56137571hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg381839
hg191839
hg181839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1889161, nssv1889167, nssv1889166, nssv1889168, nssv1889163, nssv1889164, nssv1889162, nssv1889169, nssv1889170, nssv1889165
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR5M1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975929
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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