A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975894



Internal ID18611101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:27806905..27810118hg38UCSC Ensembl
Innerchr11:27828452..27831665hg19UCSC Ensembl
Innerchr11:27785028..27788241hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg383214
hg193214
hg183214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1879012, nssv1879008, nssv1879011, nssv1879009, nssv1879007, nssv1879004, nssv1879010, nssv1879013, nssv1879006, nssv1879005
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)nsv975894
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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