A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983037



Internal ID18271545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67989171..68010919hg38UCSC Ensembl
Innerchr11:67756642..67778389hg19UCSC Ensembl
Innerchr11:67513218..67534965hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3821749
hg1921748
hg1821748
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1894654, nssv1894652, nssv1894653, nssv1894656, nssv1894659, nssv1894660, nssv1894657, nssv1894658, nssv1894655, nssv1894651
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesALDH3B1, UNC93B1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983037
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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