A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975964



Internal ID18611171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89614127..89702651hg38UCSC Ensembl
Innerchr11:89347295..89435819hg19UCSC Ensembl
Innerchr11:88986943..89075467hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3888525
hg1988525
hg1888525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1900365, nssv1900366, nssv1900364, nssv1900359, nssv1900361, nssv1900360, nssv1900367, nssv1900362, nssv1900363, nssv1900358
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFOLH1B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975964
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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