A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975875



Internal ID18611082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5967435..5968463hg38UCSC Ensembl
Innerchr11:5988665..5989693hg19UCSC Ensembl
Innerchr11:5945241..5946269hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381029
hg191029
hg181029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1874705, nssv1874708, nssv1874703, nssv1874704, nssv1874706, nssv1874710, nssv1874711, nssv1874712, nssv1874709, nssv1874707
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesOR56A5
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975875
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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