A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv983009



Internal ID18618203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47795347..47797576hg38UCSC Ensembl
Innerchr11:47816899..47819128hg19UCSC Ensembl
Innerchr11:47773475..47775704hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382230
hg192230
hg182230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1883746, nssv1883752, nssv1883750, nssv1883748, nssv1883753, nssv1883747, nssv1883755, nssv1883754, nssv1883751, nssv1883749
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNUP160
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv983009
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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