A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983034



Internal ID18618228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65025474..65027782hg38UCSC Ensembl
Innerchr11:64792946..64795254hg19UCSC Ensembl
Innerchr11:64549522..64551830hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg382309
hg192309
hg182309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1894281, nssv1894289, nssv1894288, nssv1894285, nssv1894290, nssv1894287, nssv1894282, nssv1894284, nssv1894286, nssv1894283
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesARL2-SNX15, SNX15
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983034
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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